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EFFECTIVENESS OF SOLUTION-FOCUSED APPROACH-BASED PSYCHOEDUCATION IN INDIVIDUALS DIAGNOSED WITH SUBSTANCE USE DISORDER: A RANDOMIZED CONTROLLED TRIAL

28 de julho de 2026 atualizado por: Gülten Güleşen, Okan University

Substance use disorder (SUD) is a chronic, relapsing psychiatric disorder characterized by compulsive substance use despite harmful physical, psychological, and social consequences. It is associated with impaired psychosocial functioning, reduced self-efficacy, decreased psychological well-being, and a high risk of relapse. Although detoxification, pharmacotherapy, and routine psychoeducation constitute the standard components of treatment, many individuals continue to experience difficulties maintaining recovery after discharge. Therefore, there is an increasing need for psychosocial interventions that strengthen personal resources, promote recovery, and improve long-term treatment outcomes.

The Solution-Focused Approach (SFA) is a strengths-based therapeutic model that emphasizes individuals' existing resources, successful experiences, future goals, and problem-solving abilities rather than focusing on deficits and pathology. Instead of exploring the causes of substance use, SFA encourages individuals to identify exceptions to their problems, recognize previous successes, build hope, and develop practical solutions that support behavioral change. Previous studies have suggested that solution-focused interventions may improve self-efficacy, motivation for change, coping skills, psychological well-being, and treatment engagement. However, evidence regarding the effectiveness of structured solution-focused psychoeducation programs among individuals with substance use disorder remains limited, particularly in randomized controlled trials conducted in inpatient addiction treatment settings.

The purpose of this randomized controlled trial is to evaluate the effectiveness of a structured Solution-Focused Approach-based psychoeducation program on addiction profile, self-efficacy, and psychological well-being among individuals diagnosed with substance use disorder receiving inpatient treatment.

The study was conducted between February and August 2025 at the Adult Detoxification Center of a Mental Health and Neurological Diseases Training and Research Hospital in Istanbul, Türkiye. Following completion of the detoxification phase and confirmation of eligibility criteria, participants were randomly assigned to either an intervention group or a control group. A total of 60 participants completed the study, with 30 individuals allocated to each group.

Participants assigned to the intervention group received routine inpatient treatment in addition to a structured seven-session Solution-Focused Approach-based psychoeducation program developed by the researcher according to the principles of solution-focused therapy. Each session lasted approximately 60 to 90 minutes and was delivered twice weekly in small groups. The intervention included group orientation, identification of personal strengths and resources, goal setting, miracle questions, exception finding, scaling questions, solution-focused brainstorming, future-oriented planning, relapse prevention strategies, and termination activities. Throughout the intervention, participants were encouraged to identify successful coping experiences, develop realistic future goals, recognize their existing strengths, and enhance confidence in their ability to maintain recovery.

Participants in the control group received routine inpatient addiction treatment only. Routine treatment consisted of detoxification, pharmacotherapy, therapeutic milieu interventions, psychoeducation delivered through the national SAMBA program, physician follow-up, psychiatric nursing care, family meetings, and other standard clinical services provided by the treatment center.

Outcome assessments were performed before the intervention and immediately after completion of the psychoeducation program. Data were collected using the Addiction Profile Index (BAPI), the Self-Efficacy Scale, and the Psychological Well-Being Scale. Sociodemographic and clinical characteristics were also recorded.

The primary objective of this study was to determine whether solution-focused psychoeducation improves psychological well-being and self-efficacy compared with routine inpatient treatment alone. Secondary objectives included evaluating changes in addiction profile and its subdimensions, particularly craving and safe behavioral characteristics.

It was hypothesized that participants receiving the Solution-Focused Approach-based psychoeducation program would demonstrate greater improvements in psychological well-being and self-efficacy, together with reductions in craving and addiction-related problems, compared with participants receiving routine treatment alone. The findings of this study are expected to contribute to the development of evidence-based psychosocial nursing interventions for individuals with substance use disorder and to support the integration of recovery-oriented psychoeducation into routine addiction treatment services.

Visão geral do estudo

Status

Concluído

Condições

Intervenção / Tratamento

Tipo de estudo

Intervencional

Inscrição (Real)

65

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • bakırköy
      • Istanbul, bakırköy, Turquia (Türkiye), 340000
        • Istanbul Bakirkoy Prof. Dr. Mazhar Osman Mental Health and Neurological Diseases Training and Research Hospital

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • Being 18 years of age or older with a diagnosis of Alcohol and Substance Use Disorder and having completed detoxification at the Adult Detoxification Center, having completed an average of three days of hospitalization.

Exclusion Criteria:

  • Those who want to withdraw from the study,
  • Those whose clinical condition deteriorates, those who have onset of psychotic symptoms,
  • Those who have verbal communication disorders,

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: EFFECTS OF SOLUTION-FOCUSED APPROACH-BASED PSYCHOEDUCATION ON ADDICTION PROFILE, SELF-EFFICACY AND P
psychoeducation based on solution-focused approach

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Addiction Profile Index Clinical Form (BAPI-K) Total Score
Prazo: Baseline and immediately after completion of the 7-session psychoeducation program (approximately 4 weeks)
Change in addiction severity measured using the Addiction Profile Index Clinical Form (BAPI-K). Higher scores indicate greater addiction severity. The total score will be compared between baseline and post-intervention.
Baseline and immediately after completion of the 7-session psychoeducation program (approximately 4 weeks)

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Self-Efficacy Scale Total Score
Prazo: Baseline and immediately after the 7-session psychoeducation program (approximately 4 weeks)
Change in psychological well-being measured using the Psychological Well-Being Scale. Total scores will be compared between baseline and immediately after completion of the intervention.
Baseline and immediately after the 7-session psychoeducation program (approximately 4 weeks)

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Psychological Well-Being Scale Total Score
Prazo: Baseline and immediately after the 7-session psychoeducation program (approximately 4 weeks)
Change in psychological well-being measured using the Psychological Well-Being Scale. Total scores will be compared between baseline and immediately after completion of the intervention.
Baseline and immediately after the 7-session psychoeducation program (approximately 4 weeks)

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Publicações Gerais

  • Abdollahi, Z., Taghizadeh, F., Hamzehgardeshi, Z., & Bahramzad, O. (2014). Relationship between Addiction Relapse and Self-Efficacy Rates in Injection Drug Users Referred to Maintenance Therapy Center of Sari, 1391. Global Journal of Health Science, 6(3), p138. https://doi.org/10.5539/gjhs.v6n3p138 Abram, M. D. (2018). The Role of the Registered Nurse Working in Substance Use Disorder Treatment: A Hermeneutic Study. Issues in Mental Health Nursing, 39(6), 490-498. https://doi.org/10.1080/01612840.2017.1413462 Achury-Saldaña, D., Duran De-Villalobos, M. M., & Fuentes-Ramirez, A. (2025). Self-Efficacy in People With Chronic Disease: An Evolutionary Concept Analysis. Nursing Open, 12(7), e70276. https://doi.org/10.1002/nop2.70276 Akın, A. (2008). Psikolojik İyi Olma Ölçekleri (PİOÖ): Geçerlik ve Güvenirlik Çalışması. 8(3). Ali M. (2018). Solution Focused Brief Therapy in Alcohol Dependence Syndrome [Master's Thesis]. ndia: Ranchi University Psychology Faculty, Department of Clinical Psychology. Anderson, H. (1997). Conversation, language and possibilities: A post-modern approach to therapy. APA (5th ed). (2013). American Psychiatric Publishing. Arias, A. R. L., Buss, D. F., Alburquerque, C. D., Inácio, A. F., Freire, M. M., Egler, M., Mugnai, R., & Baptista, D. F. (2007). Utilização de bioindicadores na avaliação de impacto e no monitoramento da contaminação de rios e córregos por agrotóxicos. Ciência & Saúde Coletiva, 12(1), 61-72. https://doi.org/10.1590/S1413-81232007000100011 Bagdasarian, F. A., Hansen, H. D., Chen, J., Yoo, C.-H., Placzek, M. S., Hooker, J. M., & Wey, H.-Y. (2024). Acute Effects of Hallucinogens on Functional Connectivity: Psilocybin and Salvinorin-A. ACS Chemical Neuroscience, 15(14), 2654-2661. https://doi.org/10.1021/acschemneuro.4c00245 Balster, R. L., Cruz, S. L., Howard, M. O., Dell, C. A., & Cottler, L. B. (2009). Classification of abused inhalants. Addiction, 104(6), 878-882. https://doi.org/10.1111/j.1360-0443.2008.02494.x Bandura, A. (1

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

1 de junho de 2025

Conclusão Primária (Real)

1 de junho de 2025

Conclusão do estudo (Real)

1 de junho de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

28 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

28 de julho de 2026

Primeira postagem (Real)

30 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

30 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

28 de julho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • OkanU-KO-1

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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