A Community-based Resilience Program of Only-child Loss Parents

August 28, 2023 updated by: Anni Wang, Central South University

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

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.

Study Overview

Study Type

Interventional

Enrollment (Actual)

144

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Hunan
      • Changsha, Hunan, China, 410013
        • Central South University
      • Changsha, Hunan, China, 410013
        • Yangguang Tianshi Care Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

49 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria(made according to the official documents):

  1. has given birth to only one child;
  2. now has no living birth or adopted child;
  3. the bereaved mother is older than 49 years in this family(medically maximum age for fertility in China).

Exclusion Criteria:

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Positive psychology therapy group
This arm will be given a positive psychological group intervention developed from an foreign psychotherapy.
This program is developed from a foreign group program based on positive psychology. The positive psychology therapy lasts 8 weeks, and has a group intervention in each week. The themes of each week are start-up, time gift, positive mind, three good things, a thankful heart, life train, active service, end-up.
Experimental: Resilience promotion therapy group
This arm will be given a resilience group intervention developed from our pervious research results.
The other one is developed from research team's previous research results. The resilience promotion therapy lasts 8 weeks, and also has a group intervention in each week. The themes of each week are start-up, mutual help, trust in yourself, thanksgiving feedback, care for yourself, emotional management, end-up.
Active Comparator: Controlled routine activity group
This arm will continue to participate in conventional community activities.
Conventional community activities is viewed as an active comparator for controlled group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.
Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of depression
Time Frame: Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention
Depression may refer to depressive mood in recent two weeks at each assessment measured by Zung Self-rating Depression Scale (SDS).It is a self-reported scale by adding up 20 items and the total score ranges from 20-80, with higher score reflects higher depression. The differences within time frames are changes of depression.
Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention
Change of subjective well-being
Time Frame: Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention
A feeling of happiness measured by Campbell Index of well-being (IWB).It is a self-reported scale by adding up 8 items and the total score ranges from 2.1-14.7, with higher score reflects higher subjective well-being. The differences within time frames are change of subjective well-being.
Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention
Change of social avoidance
Time Frame: Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention
The phenomenon that a person is absent from normal social interaction with others measured by Social Avoidance and Distress Scale(SAD). It is a self-reported scale by adding up 14 items and the total score ranges from 0-14, with higher score reflects social avoidance. The differences within two time frame are the changes of social avoidance.
Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention
Change of sleeping quality
Time Frame: Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention
The sleeping quality is a response of one's mood in recent month measured by Pittsburgh sleep quality index(PSQI). It is a self-reported scale, with total score higher than 19 reflects sleeping disorder. The differences within each time frames are the changes of sleeping quality.
Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention
Change of post-traumatic growth
Time Frame: Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention
The positive growth after an adversity measured by Post Traumatic Growth Inventory(PTGI). It is a self-reported scale by adding up 24 items and the total score ranges from 0-120, with higher score reflects more growth. The differences within time frames are changes of post-traumatic growth.
Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention
Change of health care behavior
Time Frame: Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention
A person's self-care behavior measured by Health Promoting Lifestyle Profile-Ⅱ( HPLP-Ⅱ).It is a self-reported scale by adding up 40 items in four dimensions. The total score ranges from 40-160, with higher score reflects better health care behavior. The differences within time frames are changes 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
Time Frame: Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention
A kind of hormone that reflects the person's psychological stress collected by Sarstedt(Brand name) saliva collection tube by chewing the sterile cotton strips for 60 seconds. It will be tested by enzyme-linked immunosorbent assay (ELISA) with Kit Number of HT81012 and Origin site in Canada PLlabs(Company name). The differences within time frames are changes of dehydroepiandrosterone concentration in saliva.
Pre-intervention, post-intervention, 3 month after finishing intervention, 1 year after finishing intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2017

Primary Completion (Actual)

January 24, 2018

Study Completion (Actual)

January 31, 2019

Study Registration Dates

First Submitted

October 19, 2017

First Submitted That Met QC Criteria

October 28, 2017

First Posted (Actual)

November 1, 2017

Study Record Updates

Last Update Posted (Actual)

August 30, 2023

Last Update Submitted That Met QC Criteria

August 28, 2023

Last Verified

August 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • Central South University

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

In our previous field investigation, most participants, as a vulnerable goup, are not willing to share their personal data to the public. Hence, we are not sure whether the recruited participants will agree to share the data.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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