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.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
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.
研究の種類
研究の種類
入学 (実際)
入学
段階
段階
- 適用できない
連絡先と場所
研究場所
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Mardin、トルコ（Türkiye）、47200
- Mardin Training and Research Hospital
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参加基準
適格基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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
研究計画
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：ヘルスサービス研究
- 割り当て：非ランダム化
- 介入モデル：並列代入
- マスキング：なし（オープンラベル）
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
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実験的：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.
他の名前：
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介入なし：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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この研究は何を測定していますか？
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Substance Craving Level
時間枠：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
時間枠：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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二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Treatment Engagement
時間枠：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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協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
研究開始
一次修了 (実際)
一次修了
研究の完了 (実際)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
その他の研究ID番号
- MAU-SBF-PSYEDU-2025-01
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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Psychoeducation Studyの臨床試験
Structured Psychoeducation Programの臨床試験
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NCT07099248まだ募集していません脳震盪 | 子供のスポーツ障害
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NCT05009095完了