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

NCT ID: NCT05703529

Last Updated: 2023-01-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

68 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-03-01

Study Completion Date

2016-10-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Resilience, Psychological Bereavement Mental Health

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Caregivers Investigators Outcome Assessors
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.

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Positive Psychotherapy group

Group Type EXPERIMENTAL

Positive Psychotherapy

Intervention Type BEHAVIORAL

A 6-week group-based positive psychotherapy was conducted in this group. The themes of each week include positive introduction, three good things and positive reactions, gratitude, positive memory, identifying personal strengths and utilizing strengths.

Control group

Usual Care means treating as usual, including a regular home visit.

Group Type OTHER

Usual Care

Intervention Type OTHER

Usual Care means treating as usual, including a regular home visit.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Positive Psychotherapy

A 6-week group-based positive psychotherapy was conducted in this group. The themes of each week include positive introduction, three good things and positive reactions, gratitude, positive memory, identifying personal strengths and utilizing strengths.

Intervention Type BEHAVIORAL

Usual Care

Usual Care means treating as usual, including a regular home visit.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Minimum Eligible Age

49 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Central South University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Zhang Wen

Xiangya School of Nursing

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2015058

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Preventing Perinatal Depression
NCT06525922 COMPLETED NA
Caregiver Stress and Sleep Study
NCT05219955 RECRUITING NA
Bounce-Back From Depression
NCT06832605 NOT_YET_RECRUITING NA