Your browser doesn't support javascript.
loading
Caring for Caregivers (C4C): study protocol for a pilot feasibility randomised control trial of Positive Written Disclosure for older adult caregivers of people with psychosis.
Hazell, Cassie M; Jones, Christina J; Hayward, Mark; Bremner, Stephen A; O'Connor, Daryl B; Pinfold, Vanessa; Smith, Helen E.
Afiliação
  • Hazell CM; Department of Primary Care and Public Health, Brighton and Sussex Medical School, Mayfield House, Village Way, Falmer, BN1 9PH UK.
  • Jones CJ; Department of Clinical Medicine, Royal Alexandra Children's Hospital, University of Sussex, Eastern Road, Brighton, BN2 5BE UK.
  • Hayward M; Sussex Partnership NHS Foundation Trust, Research and Development Department, Sussex Education Centre, Nevill Avenue, Hove, BN3 7HZ UK.
  • Bremner SA; Department of Primary Care and Public Health, Brighton and Sussex Medical School, Mayfield House, Village Way, Falmer, BN1 9PH UK.
  • O'Connor DB; School of Psychology, University of Leeds, Leeds, LS2 9JT UK.
  • Pinfold V; The McPin Foundation, 32-36 Loman Street, London, SE1 0EH UK.
  • Smith HE; Department of Primary Care and Public Health, Brighton and Sussex Medical School, Mayfield House, Village Way, Falmer, BN1 9PH UK.
Article em En | MEDLINE | ID: mdl-29201390
ABSTRACT

BACKGROUND:

The caregivers of people who experience psychosis are themselves at risk of developing physical and mental health problems. This risk is increased for older adult caregivers who also have to manage the lifestyle and health changes associated with ageing. As a consequence, older adult caregivers are in particular need of support; we propose a Written Emotional Disclosure (WED) intervention, called Positive Written Disclosure (PWD). METHODS/

DESIGN:

This is a pilot randomised controlled trial of PWD compared to a neutral writing control and a no writing condition. We aim to recruit 60 participants, 20 in each arm. This study will utilise a mixed-methods approach and collect quantitative (questionnaires) and qualitative (interviews) data. Quantitative data will be collected at baseline and 1, 3, and 6 months post baseline. Participants who complete a writing task (PWD or neutral writing control) will be invited to complete an exit interview to discuss their experiences of the intervention and study. The study is supported by a patient and public involvement group.

DISCUSSION:

The results of this trial will determine whether a definitive trial is justified. If so, the quantitative and qualitative findings will be used to refine the intervention and study protocols. TRIAL REGISTRATION ISRCTN, ISRCTN79116352. Registered on 23 January 2017.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Qualitative_research Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Qualitative_research Idioma: En Ano de publicação: 2017 Tipo de documento: Article