Clinical Trials Directory

Trials / Completed

CompletedNCT07512843

Acceptability and Efficacy of Group Reminiscence Intervention in a Sample of Patients With Schizophrenia

Evaluation of the Feasibility, Acceptability, and Preliminary Efficacy of a Group Reminiscence Intervention in a Sample of Inpatients With Schizophrenia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
38 (actual)
Sponsor
The Hashemite University · Academic / Other
Sex
All
Age
18 Years – 64 Years
Healthy volunteers
Not accepted

Summary

The study aimed to test whether group reminiscence intervention for inpatients with schizophrenia is feasible, acceptable and preliminary effective. The effect of the intervention was evaluated on cognition, communication, and social function. Phase I was a multi-phase parallel study (n=38). The purpose of the study was to assess feasibility and preliminary efficacy by conducting an 8-week intervention with the participants. The study employed a single-group pretest-posttest evaluation. Phase II evaluated acceptability and performed a thematic analysis of semi-structured interviews conducted by a purposively selected subsample (N=8).

Detailed description

The study used a sequential, multi-phase design to examine feasibility, acceptability, and preliminary efficacy of a structured group reminiscence intervention for inpatients diagnosed with schizophrenia. The intervention targeted cognitive performance, communication ability, and social functioning, domains commonly impaired in this population. Phase I applied a parallel, multi-phase approach with a sample of 38 inpatients. Participants received an 8-week group reminiscence intervention delivered in a structured format. Sessions were conducted regularly and focused on guided recall of past experiences using prompts such as life events, personal achievements, and social roles. The design followed a single-group pretest-posttest structure. Baseline measures were collected prior to the intervention, and the same outcomes were reassessed immediately after completion. Feasibility was examined through recruitment rates, retention, session attendance, and completion of outcome measures. Preliminary efficacy was assessed by comparing pre- and post-intervention scores on standardized measures of cognition, communication, and social functioning. This phase aimed to determine whether the intervention could be implemented within an inpatient psychiatric setting and whether it showed signals of benefit across targeted outcomes. Phase II focused on acceptability using a qualitative approach. A purposive subsample of eight participants from Phase I was selected to ensure variation in engagement and response to the intervention. Semi-structured interviews were conducted following completion of the program. Interview questions explored participants' experiences with the intervention, perceived benefits, challenges encountered, and suggestions for improvement. Data were analyzed using thematic analysis, allowing identification of recurring patterns related to satisfaction, perceived relevance, emotional responses, and perceived impact on interpersonal interaction and self-expression. This phase provided in-depth insight into how participants perceived the intervention and whether it was considered meaningful and appropriate in the inpatient context. The integration of quantitative findings from Phase I and qualitative insights from Phase II allowed a comprehensive evaluation of the intervention. The design supported assessment of both implementation outcomes and early indicators of clinical benefit, which are critical for informing refinement of the intervention and planning for a larger, controlled trial.

Conditions

Interventions

TypeNameDescription
BEHAVIORALGroup reminiscence therapyThe group reminiscence intervention included 8 sessions delivered over 4 weeks, with two sessions per week. Groups consisted of 3-4 participants, with 11 groups in total. Each session lasted 80-90 minutes, with careful management to limit discussion of hallucinations and delusions. Sessions followed four stages: reconnection to build rapport and trust, reflection to stimulate autobiographical recall using active listening, restating to summarize contributions, and closure emphasizing confidentiality. Trauma-informed and psychologically supportive principles guided all sessions, including sensitive handling of difficult memories. Content covered life domains such as childhood, family, and hospital experiences, with focus on coping and meaning-making. Multisensory culturally familiar stimuli were used to enhance engagement, including traditional foods, games, and music. Confidentiality was reinforced, and participants received a small appreciation gesture at the final session.

Timeline

Start date
2025-02-01
Primary completion
2025-08-29
Completion
2025-12-28
First posted
2026-04-06
Last updated
2026-04-06

Locations

1 site across 1 country: Jordan

Source: ClinicalTrials.gov record NCT07512843. Inclusion in this directory is not an endorsement.