Perceived social support and community adaptation in schizophrenia

Prompted by the continuing transition to community care, mental health nurses are considering the role of social support in community adaptation. This article demonstrates the importance of distinguishing between kinds of social support and presents findings from the first round data of a longitudinal study of community adaptation in 156 people with schizophrenia conducted in Brisbane, Australia. All clients were interviewed using the relevant subscales of the Diagnostic Interview Schedule to confirm a primary diagnosis of schizophrenia. The study set out to investigate the relationship between community adaptation and social support. Community adaptation was measured with the Brief Psychiatric Rating Scale (BPRS), the Life Skills Profile (LSP) and measures of dissatisfaction with life and problems in daily living developed by the authors. Social support was measured with the Arizona Social Support Interview Schedule (ASSIS). The BPRS and ASSIS were incorporated into a client interview conducted by trained interviewers. The LSP was completed on each client by an informal carer (parent, relative or friend) or a professional carer (case manager or other health professional) nominated by the client. Hierarchical regression analysis was used to examine the relationship between community adaptation and four sets of social support variables. Given the order in which variables were entered in regression equations, a set of perceived social support variables was found to account for the largest unique variance of four measures of community adaptation in 96 people with schizophrenia for whom complete data are available from the first round of the three-wave longitudinal study. A set of the subjective experiences of the clients accounted for the largest unique variance in measures of symptomatology, life skills, dissatisfaction with life, and problems in daily living. Sets of community support, household support and functional variables accounted for less variance. Implications for mental health nursing practice are considered.

Using images to communicate the hidden struggles of life on dialysis

Background: Nurse-patient communication in the hemodialysis context is unique given the amount of time spent together in a confined clinical room. Poor communication may lead to low quality nursing care and undesirable patient outcomes. Aim: To explore the use of images as a visual communication technique for nurses and patients in the hemodialysis context. Methods: Descriptive qualitative design. Fifty two cards containing specific photos, illustrations and words were used in conversations between patients (n = 9) and one of two nurse interviewers about being on hemodialysis. Interview transcripts were thematically analysed. Findings: An overall theme titled ‘revealing the hidden struggles of living on dialysis’ conceptually captured three sub-themes: (1) the increased importance of relationships; (2) the struggle with money; and (3) quality over quantity of life. The cards assisted in uncovering these often covert (to nurses) aspects of dialysis patients’ lives. Conclusion: Nurses may need to be aware of the dialysis patients’ hidden struggles which include the importance of relationships, financial issues and the importance of quality aspects such as travel. The use of images may assist in revealing the important issues for each patient struggling with the restrictive life that is imposed by dialysis.

Emergency Health Services (EHS) : demand and service delivery models. monograph 3 : patients’ reasons and perceptions

Executive Summary Emergency health is a critical component of Australia’s health system and emergency departments (EDs) are increasingly congested from growing demand and blocked access to inpatient beds. The Emergency Health Services Queensland (EHSQ) study aims to identify the factors driving increased demand for emergency health and to evaluate strategies which may safely reduce the future demand growth. This monograph addresses the perspectives of users of both ambulance services and EDs. The research reported here aimed to identify the perspectives of users of emergency health services, both ambulance services and public hospital Emergency Departments and to identify the factors that they took into consideration when exercising their choice of location for acute health care. A cross-sectional survey design was used involving a survey of patients or their carers presenting to the EDs of a stratified sample of eight hospitals. A specific purpose questionnaire was developed based on a novel theoretical model which had been derived from analysis of the literature (Monograph 1). Two survey versions were developed: one for adult patients (self-complete); and one for children (to be completed by parents/guardians). The questionnaires measured perceptions of social support, health status, illness severity, self-efficacy; beliefs and attitudes towards ED and ambulance services; reasons for using these services, and actions taken prior to the service request. The survey was conducted at a stratified sample of eight hospitals representing major cities (four), inner regional (two) and outer regional and remote (two). Due to practical limitations, data were collected for ambulance and ED users within hospital EDs, while patients were waiting for or under treatment. A sample size quota was determined for each ED based on their 2009/10 presentation volumes. The data collection was conducted by four members of the research team and a group of eight interviewers between March and May 2011 (corresponding to autumn season). Of the total of 1608 patients in all eight emergency departments the interviewers were able to approach 1361 (85%) patients and seek their consent to participate in the study. In total, 911 valid surveys were available for analysis (response rate= 67%). These studies demonstrate that patients elected to attend hospital EDs in a considered fashion after weighing up alternatives and there is no evidence of deliberate or ill-informed misuse. • Patients attending ED have high levels of social support and self-efficacy that speak to the considered and purposeful nature of the exercise of choice. • About one third of patients have new conditions while two thirds have chronic illnesses • More than half the attendees (53.1%) had consulted a healthcare professional prior to making the decision. • The decision to seek urgent care at an ED was mostly constructed around the patient’s perception of the urgency and severity of their illness, reinforced by a strong perception that the hospital ED was the correct location for them (better specialised staff, better care for my condition, other options not as suitable). • 33% of the respondent held private hospital insurance but nevertheless attended a public hospital ED. Similarly patients exercised considered and rational judgements in their choice to seek help from the ambulance service. • The decision to call for ambulance assistance was based on a strong perception about the severity of the illness (too severe to use other means of transport) and that other options were not considered appropriate. • The decision also appeared influenced by a perception that the ambulance provided appropriate access to the ED which was considered most appropriate for their particular condition (too severe to go elsewhere, all facilities in one spot, better specialised and better care). • In 43.8% of cases a health care professional advised use of the ambulance. • Only a small number of people perceived that ambulance should be freely available regardless of severity or appropriateness. These findings confirm a growing understanding that the choice of professional emergency health care services is not made lightly but rather made by reasonable people exercising a judgement which is influenced by public awareness of the risks of acute health and which is most often informed by health professionals. It is also made on the basis of a rational weighing up of alternatives and a deliberate and considered choice to seek assistance from a service which the patient perceived was most appropriate to their needs at that time. These findings add weight to dispensing with public perceptions that ED and ambulance congestion is a result of inappropriate choice by patients. The challenge for health services is to better understand the patient’s needs and to design and validate services that meet those needs. The failure of our health system to do so should not be grounds for blaming the patient, claiming inappropriate patient choices.

Exploring young student's functional thinking (Exploración del pensamiento funcional de estudiantes jóvenes)

The Early Years Generalizing Project (EYGP) involves Australian years 1 to 4 (age 5 to 9) students and investigates how they grasp and express generalizations. This paper focuses on data collected from 6 Year 1 students in an exploratory study within a clinical interview setting that required students to identify function rules. Preliminary findings suggest that the use of gestures (both by students and interviewers), self-talk (by students), and concrete acting out, assisted students to reach generalizations and to begin to express these generalities. It also appears that as students became aware of the structure, their use of gestures and selftalk tended to decrease.

Determinants and treatment of hypertension in South Africans: The first demographic and health survey

Objectives: To identify the groups of patients with high prevalence and poor control of hypertension in South Africa. Methods: In the first national Demographic and Health Survey, 12 952 randomly selected South Africans, aged 15 years and older were surveyed. Trained interviewers completed questionnaires on socio-demographic characteristics, lifestyle and the management of hypertension. This cross-sectional survey also included blood pressure, height and weight measurements. Logistic regression analyses identified the determinants of hypertension and the treatment status in this dataset. Results: A high risk of hypertension was associated with less than tertiary education, older age groups, overweight and obese people, using alcohol in excess, and a family history of stroke and hypertension. Rural Africans had the lowest risk of hypertension, which was significantly higher in obese African women than in women with normal body mass index. Improved hypertension control was found in the wealthy, women, older persons, being Asian, and having medical insurance. Conclusions: Rural African people had lower hypertension prevalence rates than the other groups. The poorer, younger men, without health insurance had the worst level of hypertension control.

Psykoterapian vaikutusten arvioiminen : Keskustelunanalyttinen tutkimus arviointihaastattelun käytänteistä

In the field of psychiatry semi-structured interview is one of the central tools in assessing the psychiatric state of a patient. In semi-structured interview the interviewer participates in the interaction both by the prepared interview questions and by his or her own, unstructured turns. It has been stated that in the context of psychiatric assessment interviewers' unstructured turns help to get focused information but simultaneously may weaken the reliability of the data. This study examines the practices by which semi-structured psychiatric interviews are conducted. The method for the study is conversation analysis, which is both a theory of interaction and a methodology for its empirical, detailed analysis. Using data from 80 video-recorded psychiatric interviews with 16 patients and five interviewers it describes in detail both the structured and unstructured interviewing practices. In the analysis also psychotherapeutic concepts are used to describe phenomena that are characteristic for therapeutic discourse. The data was received from the Helsinki Psychotherapy Study (HPS). HPS is a randomized clinical trial comparing the effectiveness of four forms of psychotherapy in the treatment of depressive and anxiety disorders. A total of 326 patients were randomly assigned to one of three treatment groups: solution-focused therapy, short-term psychodynamic psychotherapy, and long-term psychodynamic psychotherapy. The patients assigned to the long-term psychodynamic psychotherapy group and 41 patients self-selected for psychoanalysis were included in a quasi-experimental design. The primary outcome measures were depressive and anxiety symptoms, while secondary measures included work ability, need for treatment, personality functions, social functioning, and life style. Cost-effectiveness was determined. The data were collected from interviews, questionnaires, psychological tests, and public health registers. The follow-up interviews were conducted five times during a 5-year follow-up. The study shows that interviewers pose elaborated questions that are formulated in a friendly and sensitive way and that make relevant patients' long and story-like responses. When receiving patients' answers interviewers use a wide variety of different interviewing practices by which they direct patients' talk or offer an understanding of the meaning of patients' response. The results of the study are two-fold. Firstly, the study shows that understanding the meaning of mental experiences requires interaction between interviewer and patient. It is stated that therefore semi-structured interview is both relevant and necessary method for collecting data in psychotherapy outcome study. Secondly, the study suggests that conversation analysis, enriched with psychotherapeutic concepts, offers methodological possibilities for psychotherapy process research, especially for process-outcome paradigm.

Description of economic data collected with a random sample of commercial reef fish boats in the Florida Keys

This study summarizes the results of a survey designed to provide economic information about the financial status of commercial reef fish boats with homeports in the Florida Keys. A survey questionnaire was administered in the summer and fall of 1994 by interviewers in face-to-face meetings with owners or operators of randomly selected boats. Fishermen were asked for background information about themselves and their boats, their capital investments in boats and equipment, and about their average catches, revenues, and costs per trip for their two most important kinds of fishing trips during 1993 for species in the reef fish fishery. Respondents were characterized with regard to their dependence on the reef fish fishery as a source of household income. Boats were described in terms of their physical and financial characteristics. Different kinds of fishing trips were identified by the species that generated the greatest revenue. Trips were grouped into the following categories: yellowtail snapper (Ocyurus chrysurus); mutton snapper (Lutjanus analis), black grouper (Mycteroperca bonaci), or red grouper (Epinephelus morio); gray snapper (Lutjanus griseus); deeper water groupers and tilefishes; greater amberjack (Seriola dumerili); spiny lobster (Panulirus argus); king mackerel (Scomberomorus cavalla); and dolphin (Coryphaena hippurus). Average catches, revenues, routine trip costs, and net operating revenues per boat per trip and per boat per year were estimated for each category of fishing trips. In addition to its descriptive value, data collected during this study will aid in future examinations of the economic effects of various regulations on commercial reef fish fishermen.(PDF file contains 48 pages.)

Trazendo à baila a voz que fomenta pesquisas em linguagem: uma análise crítica do discurso do professor-orientador através do Sistema de Transitividade

A Nova Lei de Diretrizes e Bases da Educação Brasileira (LDB 9.394/96) prevê que a educação superior promova criticidade, reflexibilidade, correlação de saberes, mas também o incentivo ao trabalho de pesquisa e investigação científica, visando ao desenvolvimento da ciência e da tecnologia e da criação e difusão da cultura e, desse modo, desenvolver o entendimento do homem e do meio em que vive. (Artigo 43, inciso III). Entretanto, pouco se ouve sobre essas questões a partir da voz do orientador de pesquisas acadêmicas, o que esta pesquisadora considera um problema de ordem social, tendo em vista a importância desses atores sociais para o campo acadêmico. Os poucos trabalhos que abordam o tema limitam-se a identificar o orientador a partir das impressões empíricas dos orientandos e a refletir as atuações a partir de questões político-educacionais (FLECHA, 2003; MAZZILLI, 2003; BIANCHETTI & MACHADO, 2006). Neste sentido, o presente trabalho procura responder, através da Análise Crítica do Discurso (ACD), o que os orientadores têm a dizer sobre sua prática social. De caráter interpretativo (ALVEZ-MAZZOTTI, 1999), conta com dados gerados por orientadores de mestrado em Linguística/Linguística Aplicada, das esferas federal, estadual e privada, do Rio de janeiro, sendo dois participantes de cada esfera. Na primeira etapa, os sujeitos responderam a uma entrevista semiestruturada. A segunda etapa consta de: a) um questionário; b) correspondências eletrônicas; c) os regimentos dos programas de pós-graduação; e d) revisão histórica da orientação no Brasil. O caráter social deste estudo é a relação dialética entre linguagem e sociedade, já que a ACD considera qualquer evento discursivo ao mesmo tempo um texto (primeira dimensão), uma prática discursiva (segunda dimensão) e uma prática social (terceira dimensão): o modelo tridimensional (FAIRCLOUGH, 2001). O Sistema de Transitividade da LSF pautou a análise da primeira dimensão, confirmando outros estudos sobre o ranking da recorrência dos processos (LIMA LOPES, 2001). A interpretação dessa primeira dimensão aponta que os orientadores atuam na idiossincrasia, e que os principais atores sociais desse fazer são o orientador e o orientando, em relação assimétrica de poder. Na segunda dimensão, a interdiscursividade reforça essa idiossincrasia, mas inclui as pressões institucionais, que agem como reguladoras desse fazer. Na terceira dimensão, os resultados sugerem que aspectos históricos justificam a queda da qualidade dos mestrandos, associando a isso um interesse político, e as características da pós-modernidade a uma nova e híbrida atuação. Além disso, os resultados apontam para um discurso de resistência à hegemonia nas três dimensões de análise. A pesquisa possibilitou ainda a discussão em torno de aspectos práticos: a) a reflexão dos sujeitos sobre seus papeis e atribuições; e b) a atualização do aporte teórico, aplicado a um tema ainda pouco explorado. Deste trabalho, fica um convite a novas pesquisas sobre o discurso do orientador, trazendo à tona não apenas sua voz, conforme a fala literal de um dos entrevistados, mas também contribuições diretas e significativas aos estudos em Linguística e Linguística Aplicada no Brasil

Fatores associados ao aleitamento materno exclusivo em Juiz de Fora, MG

Este trabalho teve como objetivos identificar e analisar fatores associados ao aleitamento materno exclusivo, com significância estatística, em crianças menores de quatro meses residentes em Juiz de Fora, Minas Gerais. Fornece informações básicas para planejamento de política de amamentação neste município, estudando fatores influentes no desmame e criando Banco de Dados em Aleitamento Materno no Centro de Computação do Núcleo de Assessoria Técnica aos Estudos em Saúde da Universidade Federal de Juiz de Fora, disponível pára uso público. Compara os resultado desta pesquisa aos de outras cidades brasileiras com estudo de metodologia semelhante. Para atingir os objetivos propostos foi realizada pela autora desta tese uma pesquisa no período de 10 de agosto a 13 de setembro de 2002, época da campanha de vacinação na cidade, em uma amostra por conglomerado, tendo sido entrevistadas 1859 pessoas, sendo 625 mães e acompanhantes de crianças menores de 4 meses, em 24 postos de vacinação. A terminologia empregada deu-se de acordo com a recomendação da OMS (1991). Aplicou-se um questionário por intermédio de 268 entrevistadores voluntários, previamente treinados, incluindo estudantes da área de saúde. A pesquisa fez parte de um estudo multicêntrico em conjunto com o Núcleo de Pesquisas Epidemiológicas em Nutrição e Saúde da Universidade de São Paulo e do Núcleo de Investigação em Saúde da Mulher e da Criança, Instituto de Saúde, Secretaria Estadual de Saúde de São Paulo denominado Avaliação das práticas alimentares no primeiro ano de vida em dias nacionais de vacinação. A análise dos dados foi processada utilizando-se o programa Statiscal Package for The Social Sciences (SPSS) e os resultados foram descritos utilizando-se o teste do qui-quadrado para verificar a significância estatística da associação dos fatores independentes com o fator de desfecho aleitamento materno exclusivo. Para estudar possíveis fatores de confusão foi aplicada a técnica de análise de regressão logística. A pesquisa evidenciou que a prevalência de Aleitamento Materno Exclusivo aos 4 meses é baixa, sendo que esta é menor que as taxas da maioria das capitais brasileiras, com exceção de Cuiabá. Os hábitos de usar chupetas e mamadeiras são muito freqüentes no município. Os fatores de risco para interrupção do aleitamento materno exclusivo até os quatro meses encontrados foram: primiparidade, nascimento em hospital público ou público-privado, não disponibilidade para amamentar, uso de chupetas ou mamadeiras. A maioria das crianças inicia a amamentação no primeiro dia de vida em casa mas não de forma exclusiva. À medida que a idade aumenta, o índice de amamentação vai diminuindo progressivamente, indicando a necessidade urgente de programas de apoio e incentivo ao aleitamento materno, em especial de sua forma exclusiva, bem como de promoção do mesmo no município. Deve ser dada ênfase nesta atenção às mulheres primíparas e àquelas mulheres cujos partos ocorreram em hospitais públicos ou públicos-privados, que não tenham disponibilidade para amamentar e que utilizam mamadeiras ou chupetas para seus filhos.

As representações sociais de estudantes universitários sobre o sistema de cotas para negros e alunos de escola pública

Este estudo teve como objetivo analisar, descrever e comparar as representações sociais sobre o sistema de cotas para negros e alunos de escola pública elaboradas por estudantes universitários da UERJ, considerando a possível ocorrência de posições contranormativas na expressão dessas representações. Os estudantes participantes eram de cursos mais e menos competitivos, ingressantes e concluintes. A metodologia foi orientada pela abordagem estrutural da teoria das representações sociais. Aplicou-se a técnica das evocações livres, tendo como termos indutores cotas para negros na universidade e cotas para alunos de escola pública. Os sujeitos foram 240 estudantes, divididos igualmente por dois entrevistadores, um negro e outro branco. A partir das evocações produzidas, os dados foram analisados por meio da construção de um quadro de quatro casas, com o auxílio do software Evoc 2003. Os resultados mostram que os estudantes têm uma atitude estruturada em torno da dimensão normativa da representação, abrangendo os aspectos desfavoráveis ao sistema de cotas para negros, com os elementos racismo e preconceito como possível núcleo central. Em relação às cotas para alunos de escola pública, apresenta os elementos justo e qualidade ensino ruim, como possíveis constituintes do núcleo central. A representação foi mais consensual nesse tipo de cota, apontando para a importância da melhoria da qualidade do ensino público. Na avaliação dos diversos tipos de cotas, ocorreram diferenças nos posicionamentos diante dos aplicadores. Frente ao aplicador branco, três tipos de cotas não foram rejeitadas, as cotas para indígenas, escola pública e portadores de necessidades especiais (PNE). Entretanto, frente ao aplicador negro, observa-se que as cotas para indígenas e PNE se transformaram radicalmente. No caso das cotas para indígenas, esta atitude se justificaria pela impossibilidade de se recusar as cotas para negros e aceitar as outras modalidades de cotas com critérios raciais.

Apoio social e índice de massa corporal: um estudo de base populacional

A obesidade é uma condição de saúde que representa risco para uma série de mudanças fisiológicas e sociais ao indivíduo. O aumento de sua prevalência tanto no mundo quanto na população brasileira é considerado como um dos maiores problemas de saúde pública. A obesidade é associada com múltiplos fatores, como biológicos, individuais, ambientais e sociais, e a importância dos fatores sociais vêm sendo largamente discutida. O apoio social, que possui como uma de suas definições, a percepção de recursos disponibilizados por outros indivíduos no auxílio ao enfrentamento de situações adversas é um dos fatores sociais associados com obesidade e outros desfechos de saúde. Este constructo é um fator amplamente documentado que vem se mostrando ligado a vários desfechos de saúde nos últimos trinta anos, no entanto, existe uma lacuna sobre sua relação com o índice de massa corporal. Dessa forma, o presente estudo tem como objetivo estudar avaliar a associação entre as dimensões de apoio social e o IMC em indivíduos residentes no município de Duque de Caxias. A variável desfecho foi o IMC e as variáveis independentes, as quatro dimensões do apoio social (afetiva, material, emocional/informação e de interação social positiva). O estudo foi composto por uma amostra de 1465 indivíduos, entre 20 e 59 anos de idade, oriundos de uma pesquisa transversal de base populacional, chamada Grupo de Pesquisas sobre Segurança Alimentar e Nutricional em Duque de Caxias SANDUC. O IMC foi calculado a partir das aferições de peso e altura realizadas por entrevistadores treinados. O instrumento utilizado para avaliar o apoio social foi elaborado para o Medical Outcomes Study (MOS), tendo sido previamente adaptado para o português e validado para a população brasileira. O modelo estatístico utilizado foi a regressão linear múltipla e as análises foram realizadas através do programa SAS versão 9.3, levando em conta o fator de ponderação e o desenho de amostra complexa. Pouco mais da metade dos indivíduos eram do sexo feminino (54,94%) e a prevalência de obesidade em torno de 27,1% entre as mulheres (IC 95%: 22.4 31.8) e 16,0% (IC 95%: 12.4 19.7) entre os homens. Com relação ao apoio social, a média dos escores das dimensões situou-se entre 84 e 90 pontos, para as mulheres e para os homens, respectivamente. Entre os homens não houve associação estatisticamente significativa entre as dimensões do apoio social e o IMC (apoio afetivo: β= -0.81 e p=0.16; apoio material: β= 0.20 e p=0.72; apoio emocional/informação: β= -0.29 e p=0.61; apoio de interação social positiva: β= -0.23 e p=0.72). Porém, entre as mulheres, tanto o apoio afetivo quanto o apoio de interação social positiva mostraram associação negativa com o IMC (apoio afetivo: β= -1.02 e p=0.04; apoio de interação social positiva: β= -1.18 e p=0.01). O presente estudo sugere que, entre as mulheres, ocorre associação inversa entre o apoio social, especificamente o apoio afetivo e o de interação social positiva, e o índice de massa corporal.

Desigualdades sociais nas concepções dos professores e estudantes do PROEJA no Instituto Federal de Educação, Ciência e Tecnologia do Sertão Pernambucano - Campus Petrolina-PE

Este trabalho apresenta resultados de uma pesquisa realizada no IFSERTÃO - Instituto Federal de Educação, Ciência e Tecnologia do Sertão Pernambucano a respeito das desigualdades sociais nas concepções dos professores e estudantes do PROEJA. Teve como objetivo analisar e compreender os sentidos produzidos pelos sujeitos da pesquisa sobre as desigualdades sociais e suas perspectivas de superação, considerando seu histórico e seus aspectos atuais. Foi organizado epistemologicamente numa abordagem de pesquisa qualitativa a partir do ponto de vista metodológico do estudo de caso do tipo descritivo e analítico com entrevistas e análise do documento Base do Programa institucionalizado pelo MEC, buscando identificar as aproximações ou distanciamentos entre as concepções dos entrevistados com a proposta do material institucional no que diz respeito às perspectivas de superação das desigualdades no contexto da EJA. O problema da pesquisa foi formulado mediante o seguinte questionamento: Como as desigualdades sociais se apresentam nas concepções dos professores e estudantes do programa e quais suas perspectivas de superação? Para estudo do problema, procedeu-se à imersão no campo empírico da pesquisa com abordagens e utilização de um roteiro de entrevistas previamente formulado, incluiu-se a leitura flutuante do material coletado e as vozes dos entrevistados foram gravadas, transcritas, lidas e analisadas, buscando a captação do sentido atribuído pelos sujeitos a respeito das desigualdades sociais. Mediante essa trajetória, identificou-se, nas concepções dos sujeitos da pesquisa, que o trabalho se apresenta como centralidade no que se refere às manifestações das desigualdades sociais no contexto da EJA/PROEJA, bem como suas diferentes feições na lógica do sistema capitalista no que se refere a educar para a empregabilidade atendendo às exigências do capital. Assim, considerando que, historicamente, a EJA é uma modalidade de ensino que vem sendo ofertada para sujeitos que tiveram seus percursos escolares interrompidos pela condição de trabalhadores, esse tema se configura como estudo de grande relevância no contexto das políticas de Educação de Jovens e Adultos trabalhadores.

An evaluation of the implementation of hand held health records with adults with learning disabilities: a cluster randomized controlled trial

Background: Personal health records were implemented with adults with learning disabilities (AWLD) to try to improve their health-care. Materials and Method: Forty GP practices were randomized to the Personal Health Profile (PHP) implementation or control group. Two hundred and one AWLD were interviewed at baseline and 163 followed up after 12 months intervention (PHP group). AWLD and carers of AWLD were employed as research interviewers. AWLD were full research participants. Results: Annual consultation rates in the intervention and control groups at baseline were low (2.3 and 2.6 visits respectively). A slightly greater increase occurred over the year in the intervention group 0.6 ()0.4 to 1.6) visits ⁄ year compared with controls. AWLD in PHP group reported more health problems at follow-up 0.9 (0.0 to 1.8). AWLD liked their PHP (92%) but only 63% AWLD and 55% carers reported PHP usage. Carers had high turnover (34%). Conclusions: No significant outcomes were achieved by the intervention.

Participation of 8-12 year old children with cerebral palsy: a cross-sectional European Survey

Objectives
To evaluate how involvement in life situations (participation) in children with cerebral palsy varies with type and severity of impairment and to investigate geographical variation in participation.

Design
Cross sectional study. Trained interviewers visited parents of children with cerebral palsy; multilevel multivariable regression related participation to impairments, pain, and sociodemographic characteristics.

Setting
Eight European regions with population registers of children with cerebral palsy; one further region recruited children from multiple sources.

Participants
1174 children aged 8-12 with cerebral palsy randomly selected from the population registers, 743 (63%) joined in the study; the further region recruited 75 children.

Main outcome measure
Children’s participation assessed by the Life-H questionnaire covering 10 main areas of daily life. Scoring ignored adaptations or assistance required for participation.

Results
Children with pain and those with more severely impaired walking, fine motor skills, communication, and intellectual abilities had lower participation across most domains. Type of cerebral palsy and problems with feeding and vision were associated with lower participation for specific domains, but the sociodemographic factors examined were not. Impairment and pain accounted for up to a sixth of the variation in participation. Participation on all domains varied substantially between regions: children in east Denmark had consistently higher participation than children in other regions. For most participation domains, about a third of the unexplained variation could be ascribed to variation between regions and about two thirds to variation between individuals.

Conclusions
Participation in children with cerebral palsy should be assessed in clinical practice to guide intervention and assess its effect. Pain should be carefully assessed. Some European countries facilitate participation better than others, implying some countries could make better provision. Legislation and regulation should be directed to ensuring this happens.

A pilot study of a family focused, psychosocial intervention with war-exposed youth at risk of attack and abduction in north-eastern Democratic Republic of Congo

Rural communities in the Haut-Uele Province of northern Democratic Republic of Congo live in constant danger of attack and/or abduction by units of the Lord's Resistance Army operating in the region. This pilot study sought to develop and evaluate a community-participative psychosocial intervention involving life skills and relaxation training and Mobile Cinema screenings with this war-affected population living under current threat. 159 war-affected children and young people (aged 7-18) from the villages of Kiliwa and Li-May in north-eastern DR Congo took part in this study. In total, 22% of participants had been abduction previously while 73% had a family member abducted. Symptoms of post-traumatic stress reactions, internalising problems, conduct problems and pro-social behaviour were assessed by blinded interviewers at pre- and post-intervention and at 3-month follow-up. Participants were randomised (with an accompanying caregiver) to 8 sessions of a group-based, community-participative, psychosocial intervention (n=79) carried out by supervised local, lay facilitators or a wait-list control group (n=80). Average seminar attendance rates were high: 88% for participants and 84% for caregivers. Drop-out was low: 97% of participants were assessed at post-intervention and 88% at 3 month follow-up. At post-test, participants reported significantly fewer symptoms of post-traumatic stress reactions compared to controls (Cohen's d=0.40). At 3 month follow up, large improvements in internalising symptoms and moderate improvements in pro-social scores were reported, with caregivers noting a moderate to large decline in conduct problems among the young people. Trial Registration clinicalTrials.gov, Identifier: NCT01542398.