Resourcefulness Group Intervention on Recovery and Quality of Life
The Effects of Resourcefulness Group Intervention on Recovery and Quality of Life in Patients With Chronic Schizophrenia.
1 other identifier
interventional
40
1 country
1
Brief Summary
The purpose of this study was to test the effects of resourcefulness group intervention on facilitating recovery and improving the quality of life in patients with chronic schizophrenia.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2022
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 6, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 14, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
September 14, 2022
CompletedFirst Submitted
Initial submission to the registry
August 9, 2023
CompletedFirst Posted
Study publicly available on registry
January 16, 2024
CompletedJanuary 16, 2024
January 1, 2024
3 months
August 9, 2023
January 4, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Chinese version of Resourcefulness Scale
Resourcefulness
Up to 10 weeks. The pre-test questionnaire will be completed before the group starts, the first post-test will be administered after the group, and the second post-test will be administered 4 weeks after the group ends
Chinese questionnaire about the process of recovery
recovery
Up to 10 weeks. The pre-test questionnaire will be completed before the group starts, the first post-test will be administered after the group, and the second post-test will be administered 4 weeks after the group ends
WHOQOL-BREF Taiwan version
Quality of Life
Up to 10 weeks. The pre-test questionnaire will be completed before the group starts, the first post-test will be administered after the group, and the second post-test will be administered 4 weeks after the group ends
Study Arms (2)
experimental group
EXPERIMENTAL1. Subjects were randomly assigned to the experimental or the control group. 2. There were 20 members in the experimental group who received 6-week intervention activities. 3. Each subject was asked to fill out the questionnaires three times in total. The first time was before the intervention; the second time was right after the intervention; and the last time was four weeks later of the intervention.
control group
NO INTERVENTION1. There were 20 members in the control group who accepted chronic nursing care as usual without any nursing intervention. 2. Each subject was asked to fill out the questionnaires three times in total. The first time was the same time as the experimental group; the second time was 6 weeks after the first test; and the last time was four weeks after the second test.
Interventions
The content of the Resourcefulness intervention group includes 6 sessions such as session 1 to introduce resourcefulness skills; sessions 2-4 to discuss personal resourcefulness skills including planning daily activities, and positive self-talk; sessions 4-5 to discuss social resourcefulness skills including relying on family or friends, and seeking professional assistance.
Eligibility Criteria
You may qualify if:
- Subjects who have been diagnosed with schizophrenia by a psychiatrist for more than two years and are currently receiving rehabilitation treatment in a chronic ward.
- Age between 20-64 years old.
- Those with stable conditions can communicate in Mandarin or Taiwanese.
You may not qualify if:
- Exclude clients with Intellectual Disabilities, Organic Encephalopathy, Substance-related and addictive disorders, Personality disorders, Dementia, Cancers, etc.
- Those who are unable to understand the contents of the consent form.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Peihsin Hospital
New Taipei City, Tamsui Dist, 251010, Taiwan
Study Officials
- STUDY DIRECTOR
Chien Yu Lai, PhD.
Associate professor
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- INVESTIGATOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- graduate student
Study Record Dates
First Submitted
August 9, 2023
First Posted
January 16, 2024
Study Start
June 6, 2022
Primary Completion
September 14, 2022
Study Completion
September 14, 2022
Last Updated
January 16, 2024
Record last verified: 2024-01
Data Sharing
- IPD Sharing
- Will not share