跳至主要内容
临床试验/NCT03446963
NCT03446963已完成不适用

Feasibility Study of the Groups for Health Intervention for Adults Accessing Treatment for Depression

University of Nottingham2 个研究点 分布在 1 个国家目标入组 29 人开始时间: 2018年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
29
试验地点
2
主要终点
Feasibility of data collection

研究概览

简要总结

This study evaluates the feasibility of the Groups for Health (G4H) intervention for adults accessing support for depression in the UK. G4H targets improvements in adults' interpersonal functioning in order to reduce feelings of loneliness. The study will adapt the G4H intervention for delivery to adults seeking treatment for depression in the UK and estimate trial parameters (recruitment, retention, missing data and acceptability) of the adapted intervention, prior to a definitive trial. A mixed methods design of interviews and a single group, pre-post study will be employed.

详细描述

Background: Loneliness is frequently reported amongst adults with depression. Interventions to reduce loneliness in different populations have shown mixed results. The Groups for Health (G4H) programme has been developed according to the social identity approach within social psychology and has demonstrated preliminary efficacy for reducing loneliness in a proof-of-concept study conducted with Australian student sample. The present study will examine whether G4H can be adapted to suit the needs of a clinical population in the context of UK secondary care services.

Objective

Phase 1 - To adapt the G4H intervention for delivery to adults seeking treatment for depression in the UK. Phase 2: To estimate trial parameters (recruitment, retention, missing data and acceptability) of the adapted intervention, prior to a definitive trial; to optimise the adapted intervention for delivery to adults accessing treatment for depression in the UK; to optimise evaluation procedures (candidate outcome measures)

Trial configuration: sequential exploratory mixed methods design. Phase 1: one-to-one interviews. Phase 2: Activity 1 (intervention), single group, pre-post study. Activity 2 (interviews): one-to-one interviews.

Condition: Depression

Interventions: group-based behavioural programme

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Service user participants:
  • Aged 18-65
  • Accessing treatment for depression
  • Loneliness: score 6 or above on the University of California Loneliness Scale (UCLA-3) (Hughes et al., 2004)
  • Able to speak/read English
  • Ability to give informed consent
  • Staff participants:
  • Clinical practitioner with at least 6 months experience of working with people with depression
  • Phase 2 Activity 1: intervention
  • Aged 18-65
  • Accessing treatment for depression
  • Loneliness: score 6 or above on the University of California Loneliness Scale (UCLA-3) (Hughes et al., 2004)
  • Able to speak/read English
  • Ability to give informed consent
  • Activity 2: interviews
  • Attended or agreed to attend Phase 2, Activity 1

排除标准

  • 未提供

研究组 & 干预措施

Single arm: Groups 4 Health

Experimental

Social group intervention. The aim is to practice participating in a social group within a safe environment; to identify groups and social networks which are meaningful for the person; and to understand any barriers people may have to engaging with these groups/networks.

干预措施: Groups for Health (Behavioral)

结局指标

主要结局

Feasibility of data collection

时间窗: 8 weeks

The overall proportion of survey measures completed by each participant at each of the 2 time points

Feasibility of recruitment

时间窗: 3 months

The proportion of patients contacted for screening against those who are consented

Patient retention

时间窗: 8 weeks

The proportion of patients attending all five G4H sessions

Feasibility of enrollment

时间窗: 3 months

The proportion of patients consented against those enrolled

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验