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This randomized controlled study aims to evaluate the effects of a Solution-Focused Brief Therapy (SFBT)-based structured program on hope, problem-solving skills, and life satisfaction among students attending a university vocational school. Fifty eligible students from two campuses of a state university will be randomized to an intervention group (n=25) or a control group (n=25). The intervention group will receive a structured SFBT-based program delivered face-to-face, while the control group will continue usual conditions during the study period. Outcomes will be assessed using standardized questionnaires at baseline, post-intervention, and follow-up. The primary analyses will compare changes in outcome scores over time between groups.
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Aim: The aim of this study is to examine the effects of Solution-Focused Brief Therapy (SFBT) delivered to associate degree students on hope, problem-solving skills, and life satisfaction.
Design: This is a parallel-group randomized controlled experimental study. Setting: The study will be conducted at a state university vocational school located on two separate campuses.
Participants and sample size: The planned sample size is 50 university students, with approximately 25 participants in the intervention group and 25 in the control group.
Intervention: The intervention group will receive a structured, face-to-face SFBT-based brief program focusing on goal setting, identifying exceptions, scaling questions, and strengthening personal resources and small-step planning.
Control: The control group will continue usual conditions and will not receive the SFBT program during the study period.
Outcome measures: Data will be collected using a Personal Information Form, the Continuous Hope Scale (CHS), the Problem Solving Inventory (PSI), and the Life Satisfaction Scale (LSS). Outcomes will be assessed at baseline (T0), post-intervention (T1), and follow-up (T2).
Statistical analysis: Data will be analyzed using appropriate descriptive statistics and repeated-measures approaches to compare changes over time between groups. The significance level will be specified a priori.
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46 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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