Effect Of Psychoeducation On Substance Craving Levels And Psychological Resilience
Effect Of Psychoeducation On Substance Craving Levels And Psychological Resilience İn Patients With Substance Use Disorder Under Probation Supervision
What is known on the subject? Substance use disorder is a chronic condition with high relapse risk, and individuals under probation supervision are particularly vulnerable. Psychoeducation and psychological resilience are important factors in reducing craving and improving treatment outcomes.
What the paper adds to existing knowledge
What are the implications for practice? Psychoeducation can be effectively used by psychiatric nurses in probation settings to support recovery. Strengthening psychological resilience should be considered a key target in addiction interventions.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Introduction: Substance use disorder is a major public health problem that adversely affects individuals' physical, psychological, and social functioning. For individuals under probation supervision, preventing relapse and controlling substance use are of critical importance. Psychoeducation is an important psychosocial intervention with the potential to reduce craving and enhance psychological resilience.
Aim: This study aimed to examine the effect of psychoeducation on substance craving levels and psychological resilience in individuals diagnosed with substance use disorder under probation supervision.
Methods: A quasi-experimental pretest-posttest control group design was used. The study included 60 participants (30 intervention, 30 control). A structured psychoeducation program was applied to the intervention group, while the control group continued to receive standard care. Data were collected using a personal information form, the substance craving scale, and the Adult Resilience Scale.
Discussion: Psychoeducation is thought to reduce substance craving and increase psychological resilience by strengthening cognitive and emotional regulation in the addiction process.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Mardin, Turquía (Türkiye), 47200
- Mardin Training and Research Hospital
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Being 18 years of age or older
- Being under probation supervision
- Having a diagnosis of substance use disorder according to DSM-5
- Being able to attend psychoeducation sessions regularly
- Providing written informed consent
- Not having participated in a similar psychoeducation program within the past 6 months
Exclusion Criteria:
- Diagnosis of schizophrenia, severe psychotic disorder, or cognitive impairment
- Being in an acute withdrawal period
- Inability to attend sessions regularly
- Presence of severe communication or behavioral disorders
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Investigación de servicios de salud
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Experimental
A structured psychoeducation program was administered to individuals with substance use disorder under probation supervision.
The program included six weekly sessions focusing on relapse prevention, coping strategies, psychological resilience, and substance craving management.
The intervention was delivered by a trained mental health professional over a six-week period, with one 60-minute session per week.
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A structured psychoeducation program was implemented for individuals with substance use disorder under probation supervision.
The program focused on relapse prevention, coping strategies, psychological resilience, and craving management.
It was delivered in weekly group sessions over six weeks by a trained mental health professional in a hospital setting.
Each session lasted 60 minutes.
The intervention was designed to support rehabilitation and treatment processes in outpatient probation services.
Otros nombres:
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Sin intervención: Control
During the study period, no intervention or psychoeducation program was applied to the participants in the control group.
Individuals in this group were monitored solely within the scope of routine probation procedures and were subjected only to pre-test and post-test measurements.
Throughout the intervention period, the data of the control group were evaluated within the natural course, without any additional educational or psychosocial intervention.
Upon completion of the study, in accordance with ethical principles, it was stated that the same psychoeducation program would be offered to participants who requested it.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Substance Craving Level
Periodo de tiempo: Baseline (pre-intervention) and immediately after the 6-week intervention
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Psychological resilience was measured using a validated resilience scale .
Higher scores indicate greater resilience.
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Baseline (pre-intervention) and immediately after the 6-week intervention
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Psychological Resilience
Periodo de tiempo: Baseline (pre-intervention) and immediately after the 6-week intervention
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Psychological resilience was measured using a validated resilience scale .Higher scores indicate greater resilience.
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Baseline (pre-intervention) and immediately after the 6-week intervention
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Treatment Engagement
Periodo de tiempo: During the 6-week intervention period
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Attendance and participation rates in psychoeducation sessions were recorded to evaluate program adherence.
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During the 6-week intervention period
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- MAU-SBF-PSYEDU-2025-01
Información sobre medicamentos y dispositivos, documentos del estudio
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