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Clinical Trials/NCT05703529
NCT05703529
Completed
N/A

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

Central South University0 sites68 target enrollmentMarch 1, 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Resilience, Psychological
Sponsor
Central South University
Enrollment
68
Primary Endpoint
Change of psychological resilience
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
March 1, 2016
End Date
October 31, 2016
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Central South University
Responsible Party
Principal Investigator
Principal Investigator

Zhang Wen

Xiangya School of Nursing

Central South University

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

  • 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.

Outcomes

Primary Outcomes

Change of psychological resilience

Time Frame: 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.

Secondary Outcomes

  • 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)

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