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NCT Number: NCT07144592

The Effects of a Solution-Focused Approach on Psychosocial Adjustment and Treatment Compliance in Individuals Diagnosed With Schizophrenia

The aim of this study is to evaluate the effects of a solution-focused approach-based individual intervention on psychosocial adjustment and treatment adherence in individuals diagnosed with schizophrenia.

The study will be conducted as a randomized controlled trial including 60 clinically stable individuals diagnosed with schizophrenia according to DSM-5 criteria and registered at a Community Mental Health Center affiliated with a university hospital. Participants will be randomly assigned to an experimental group (n=30) and a control group (n=30).

The experimental group will receive one individual solution-focused therapy session per week for six weeks. The control group will receive usual care only. Data will be collected using a Personal Information Form, the Psychosocial Adjustment Scale (PSSAS), and the Medication Adherence Scale (MARS).

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Community Mental Health Center

Muş, Turkey (Türkiye)

Location status: Recruiting

Location contact

muş alparsalan üniversity University

CONTACT

[email protected]

0346 249 4949

About this study

Objective:

Schizophrenia is a chronic psychiatric disorder that significantly affects thought, emotion, and behavior, often limiting social functioning, treatment adherence, and integration into daily life. There is an increasing need for person-centered, empowering, and brief intervention models in psychiatric nursing. This study aims to determine the effects of a solution-focused approach (SFA)-based individual intervention on psychosocial adjustment and treatment adherence in individuals with schizophrenia.

Study Design:

This research will use a pretest-posttest randomized controlled experimental design with a control group.

Study Population:

The study will include 60 individuals diagnosed with schizophrenia according to DSM-5 diagnostic criteria, considered clinically stable, and registered at a Community Mental Health Center affiliated with a university hospital in Türkiye. Participants will be randomly assigned to an experimental group (n=30) or a control group (n=30) using computer-assisted randomization.

Intervention:

Experimental Group: Participants will receive individual solution-focused therapy sessions once per week for six consecutive weeks. The sessions will emphasize individual strengths, recall positive coping experiences, support future goal setting, and provide guidance on repeating effective solutions.

Control Group: Participants will receive no additional intervention beyond usual care.

Outcome Measures:

Data will be collected with the following instruments:

Personal Information Form

Psychosocial Adjustment Scale (PSSAS)

Medication Adherence Scale (MARS)

Statistical Analyses:

Planned analyses will include independent samples t-tests, paired t-tests, and ANCOVA.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Having been diagnosed with schizophrenia according to DSM-5 diagnostic criteria,

Being between 18 and 65 years of age,

Being literate and verbally communicative,

Being clinically stable (not exhibiting symptoms of acute psychosis),

Being registered with a Community Mental Health Center (CMHC) and receiving regular services,

Being cognitively competent enough to participate in individual interviews during the research process,

Being an individual currently receiving psychiatric treatment and taking medication,

Agreeing to participate voluntarily in the study and signing a written informed consent form.

Exclusion criteria

  • those who do not meet the inclusion criteria

Treatment and study plan

solution-oriented approach program

Behavioral

The solution-focused nursing intervention applied to the experimental group in the study was planned as individual sessions, consisting of one session per week, lasting a total of six weeks. The interventions were based on the principles of solution-focused brief therapy, focusing on the individual's strengths, past coping experiences, and current resources. The interviews aimed to identify exceptions, build positive future expectations, set small but achievable goals, strengthen hope, and increase the individual's ability to utilize their internal resources. Each session used structured open-ended questions, scaling techniques, and future-oriented solution scenarios to support the individual's psychosocial adjustment and motivation for treatment.

Primary outcomes

  1. pretest (6-week solution-focused approach before the intervention)

    Time frame: Baseline (1 week before intervention)]

    • Psychosocial Adjustment (PSSAS)

    Description: Measured with the Psychosocial Adjustment Scale (PSSAS), which assesses social relationships, daily life management, and coping with stress. Scores range from 0 to 180; higher scores indicate better psychosocial adjustment.

    Time Frame: Baseline (within 1 week before intervention)

    Unit of Measure: Total score (0-180)

  2. pretest (6-week solution-focused approach before the intervention)

    Time frame: Baseline (within 1 week before intervention)

    • Medication Adherence (MARS)

    Description: Measured with the Medication Adherence Scale (MARS), which assesses adherence to prescribed pharmacological treatment. Scores range from 0 to 10; higher scores indicate better medication adherence.

    Time Frame: Baseline (within 1 week before intervention)

    Unit of Measure: Total score (0-10)

Secondary outcomes

  1. posttest (After the 6-week solution-focused approach intervention)

    Time frame: 6 weeks after baseline (post-intervention)

    • Psychosocial Adjustment Post-Intervention (PSSAS)

    Description: Psychosocial Adjustment Scale (PSSAS). Scores range from 0 to 180; higher scores indicate better psychosocial adjustment.

    Time Frame: 6 weeks after baseline (post-intervention)

    Unit of Measure: Total score (0-180)

  2. posttest (After the 6-week solution-focused approach intervention)

    Time frame: Post-intervention (6 weeks after completion of the intervention)

    • Medication Adherence Post-Intervention (MARS)

    Description: Medication Adherence Scale (MARS). Scores range from 0 to 10; higher scores indicate better medication adherence.

    Time Frame: Post-intervention (6 weeks after completion of the intervention)

    Unit of Measure: Total score (0-10)

Study contacts

Contact information is provided by the study sponsor or research team.

Fatih Şahin, dr

CONTACT

[email protected]

0534 688 1634

Sponsors and collaborators

Lead sponsor

Muş Alparslan University

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Aug 27, 2025
Registry last updated
Aug 27, 2025

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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