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Completed

NCT Number: NCT06206798

Resourcefulness Group Intervention on Recovery and Quality of Life

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.

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Key information

Age range

20 year–64 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Peihsin Hospital

New Taipei City, Tamsui Dist, 251010, Taiwan

About this study

Purpose: This study aimed to explore the effects of resourcefulness group intervention on facilitating recovery and improving the quality of life in patients with chronic schizophrenia.

Methods: A longitudinal and interventional study with a quasi-experimental research design and convenience sampling were used in this study. Patients with chronic schizophrenia from a psychiatric hospital in northern Taiwan were recruited as subjects and were divided under random assignment into the experimental group and the control group with twenty participants in each. The twenty participants in the experiment group were further randomly distributed into two groups. Both received resourcefulness group intervention weekly for six weeks, while the control group followed regular care routines and underwent conventional treatment. All participants took a pretest before the intervention, the first posttest after six rounds of intervention, and the second posttest four weeks after the group intervention was completed. Data were collected using structured questionnaires, including the Chinese version of the Resourcefulness Scale (C-RS), the Chinese Questionnaire about the Process of Recovery (QPR), the WHOQOL-BREF Taiwan Version, and other personal information.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Treatment and study plan

Resourcefulness Group

Behavioral

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.

Primary outcomes

  1. Chinese version of Resourcefulness Scale

    Time frame: 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

    Resourcefulness

  2. Chinese questionnaire about the process of recovery

    Time frame: 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

    recovery

  3. WHOQOL-BREF Taiwan version

    Time frame: 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

    Quality of Life

Sponsors and collaborators

Lead sponsor

National Taipei University of Nursing and Health Sciences

Other

Registry information

Official study title

The Effects of Resourcefulness Group Intervention on Recovery and Quality of Life in Patients With Chronic Schizophrenia.

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Jan 16, 2024
Registry last updated
Jan 16, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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