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Clinical Trials/NCT03328598
NCT03328598
Terminated
Not Applicable

Implementation of a Community-based Resilience Promotion Program to Only-child Loss Parents in China

Central South University2 sites in 1 country144 target enrollmentDecember 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Resilience,Psychological
Sponsor
Central South University
Enrollment
144
Locations
2
Primary Endpoint
Change of psychological resilience
Status
Terminated
Last Updated
2 years ago

Overview

Brief Summary

This is a community-based participatory research aiming at helping the only-child loss parents to be happier and resilient from bereavement. It is a psycho-behavioral intervention research. There are two intervention programs in this study. One is derived from a foreign psychotherapy, developed by an American psychologist and has been testified the effectiveness in promoting happiness. Another one is developed by the researchers based on the previous cross-sectional survey and interviews with those bereaved parents. The researchers will apply randomized controlled trial to testify and compare those two intervention programs in a Chinese community.

Registry
clinicaltrials.gov
Start Date
December 1, 2017
End Date
January 31, 2019
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Central South University
Responsible Party
Principal Investigator
Principal Investigator

Anni Wang

Dr.

Central South University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • with serious mental disorders or physical illnesses;
  • are not able to complete the intervention;
  • are not able to finish questionnaire;
  • with chewing functional disorder to collect saliva dehydroepiandrosterone.

Outcomes

Primary Outcomes

Change of psychological resilience

Time Frame: Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention

Psychological resilience is a kind of ability to bounce back from adversity measured by Connor-Davidson Resilience Scale (CD-RISC).It is a self-reported scale by adding up 25 items and the total score ranges from 0-100, with higher score reflects higher resilience. The differences within two times frame are the changes of psychological resilience.

Secondary Outcomes

  • Change of subjective well-being(Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention)
  • Change of depression(Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention)
  • Change of social avoidance(Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention)
  • Change of post-traumatic growth(Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention)
  • Change of sleeping quality(Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention)
  • Change of health care behavior(Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention)
  • Change of concentration of dehydroepiandrosterone in saliva(Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention)

Study Sites (2)

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