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临床试验/NCT05703529
NCT05703529已完成不适用

The Impact of Group-based Positive Psychotherapy in Psychological Resilience of Only-child-lost People: A Randomized Controlled Trial

Central South University0 个研究点目标入组 68 人开始时间: 2016年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
68
主要终点
Change of psychological resilience

研究概览

简要总结

A randomized controlled trial was conducted to evaluate the effectiveness of group-based positive psychotherapy on psychological resilience, depression, well-being, sleep quality, dehydroepiandrosterone in only-child-lost people. A total of 80 only-child-lost people who met the inclusion and exclusion criteria were expected to recruit. There were six weeks in the intervention, including positive introduction, positive reaction, gratitude, meaningful, three good things, and using personal strength. The measurements were conducted at the baseline, immediately after the intervention, 3-month after the intervention.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Care Provider, Investigator, Outcomes Assessor)

盲法说明

The intervention provider, investigator, and outcomes assessor have not been informed of the group allocation, but the participants may be aware of the group allocation because of the nature of the research design.

入排标准

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

入选标准

  • having only one child or legally adopting;
  • No surviving children;
  • basic language expression and comprehension skills;
  • the score of Connor-Davidson Resilience Scale is lower than 82

排除标准

  • in the acute bereavement period (<6 months);
  • unable to participate in activities due to severe physical illness;
  • having diagnosis of sever mental illness;
  • receiving other psychological therapy.

结局指标

主要结局

Change of psychological resilience

时间窗: Baseline, immediately after the intervention, 3-month after the intervention

It is assessed by Connor-Davidson Resilience Scale. A higher score suggests a higher level of psychological resilience. The range is 0-100.

次要结局

  • Change of depressive symptoms(Baseline, immediately after the intervention, 3-month after the intervention)
  • Change of index of well-being(Baseline, immediately after the intervention, 3-month after the intervention)
  • Change of Dehydroepiandrosterone (DHEA) in saliva(Baseline, immediately after the intervention, 3-month after the intervention)
  • Change of Sleep Quality(Baseline, immediately after the intervention, 3-month after the intervention)
  • Change of Social Avoidance and Social Distress(Baseline, immediately after the intervention, 3-month after the intervention)

研究者

发起方
Central South University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Zhang Wen

Xiangya School of Nursing

Central South University

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