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Group-based Positive Psychotherapy in Psychological Resilience of Only-Child-Lost People

Not Applicable
Completed
Conditions
Bereavement
Mental Health
Resilience, Psychological
Interventions
Other: Usual Care
Behavioral: Positive Psychotherapy
Registration Number
NCT05703529
Lead Sponsor
Central South University
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
68
Inclusion Criteria
  1. having only one child or legally adopting;
  2. No surviving children;
  3. basic language expression and comprehension skills;
  4. the score of Connor-Davidson Resilience Scale is lower than 82
Exclusion Criteria
  1. in the acute bereavement period (<6 months);
  2. unable to participate in activities due to severe physical illness;
  3. having diagnosis of sever mental illness;
  4. receiving other psychological therapy.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control groupUsual CareUsual Care means treating as usual, including a regular home visit.
Positive Psychotherapy groupPositive Psychotherapy-
Primary Outcome Measures
NameTimeMethod
Change of psychological resilienceBaseline, 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 Outcome Measures
NameTimeMethod
Change of depressive symptomsBaseline, immediately after the intervention, 3-month after the intervention

It is measured by Zung Self-rating Depression Scale with a higher score suggesting a more severe of depressive symptoms

Change of index of well-beingBaseline, immediately after the intervention, 3-month after the intervention

It is measured by Campbell's Index of Well-being. A high score indicates a high level of well-being.

Change of Dehydroepiandrosterone (DHEA) in salivaBaseline, immediately after the intervention, 3-month after the intervention

Saliva is collected using a saliva collector and assayed using the Elisa assay. After the specimens were collected, they were tested with the Elisa kit of Salimetrics® according to its instructions.

Change of Sleep QualityBaseline, immediately after the intervention, 3-month after the intervention

It is measured by Pittsburgh Sleep Quality Index. If the total score is over 7, the sleep quality is normal, and if the score is over 7, it suggests a low sleep quality

Change of Social Avoidance and Social DistressBaseline, immediately after the intervention, 3-month after the intervention

It is measured by Social Avoidance and Distress Scale. A high score indicates a high level of social avoidance and social distress.

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