NCT06206798

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 14, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 14, 2022

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

August 9, 2023

Completed
5 months until next milestone

First Posted

Study publicly available on registry

January 16, 2024

Completed
Last Updated

January 16, 2024

Status Verified

January 1, 2024

Enrollment Period

3 months

First QC Date

August 9, 2023

Last Update Submit

January 4, 2024

Conditions

Keywords

ResourcefulnessChronic SchizophreniaResourcefulness GroupRecoveryQuality of Life

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

EXPERIMENTAL

1. 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.

Behavioral: Resourcefulness Group

control group

NO INTERVENTION

1. 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.

experimental group

Eligibility Criteria

Age20 Years - 64 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

Location

Study Officials

  • Chien Yu Lai, PhD.

    Associate professor

    STUDY DIRECTOR

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

Locations