Effectiveness of Group-based Positive Psychotherapy and Positive Cognitive Behavioral Therapy in Improving Psychological Distress, Coping Strategies, and Well-being Among Incarcerated Individuals. (GB- PPT&PCBT)
Effectiveness of Group-based Positive Psychotherapy and Positive Cognitive Behavioral Therapy in Improving Psychological Distress, Coping Strategies, and Well-being Among Incarcerated Individuals
The foremost idea of the proposed research is to highlight the impact of psychological distress and coping strategies on the wellbeing of individuals in incarceration. In Pakistan, there is limited literature available to support the psychological wellbeing of individuals in incarceration. The current research will not only explore the impact of psychological distress and coping strategies on the wellbeing of inmates. In addition, the research will also aim to investigate the effectiveness of group-based interventions, which includes Positive Psychotherapy (PPT) and Positive Cognitive Behavioral Therapy (PCBT) in improving psychological distress, coping strategies, and wellbeing of Incarcerated Individuals.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- 適用できない
連絡先と場所
研究場所
-
-
Sindh
-
Karachi、Sindh、パキスタン
- 完了
- Central Prison and Correctional Facility for Women Karachi
-
Karachi、Sindh、パキスタン
- 積極的、募集していない
- Central Prison and Correctional Facility Karachi
-
Karachi、Sindh、パキスタン
- 募集
- District Prison & Correctional Facility Malir Karachi
-
コンタクト：
- Bilawal Khumbar ASP
- 電話番号：009221-99231418
- メール：sindhprisons@gmail.com
-
Karachi East、Sindh、パキスタン
- 積極的、募集していない
- Youthful Offenders Industrial School (YOIS)
-
-
参加基準
適格基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Individuals with first time offense
- Minimum duration of incarceration: 3 months.
- Must have a score falling in the mild to severe range for depression and/or anxiety and a score below 6.4 on the PERMA profiler.
- Urdu understanding and ability to comprehend measures
Exclusion Criteria:
- not falling in the age criteria
- having a history of repeated crime
- under any pharmacological and psychological treatment.
- Individuals with types of crimes such as murder and rape were not included.
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：処理
- 割り当て：ランダム化
- 介入モデル：並列代入
- マスキング：独身
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 |
|---|---|
|
実験的：Positive Psychotherapy (PPT)
The participants in this experimental group will receive intervention; treatment plan based on a strong foundation of positive psychology for enhancing positive emotions, engagement, relationships, meaning, and accomplishment by building up individuals' inner skill sets, including strengths and achievements, to manage their psychological distress to improve their quality of life. |
The participants in this experimental group will receive intervention; treatment plan based on a strong foundation of positive psychology for enhancing positive emotions, engagement, relationships, meaning, and accomplishment by building up individuals' inner skill sets, including strengths and achievements, to manage their psychological distress to improve their quality of life. The intervention plan is designed to employ 8 PPT exercises, including a positive introduction, three good things, using character strengths in a way, positive cognitive reappraisal, active constructive responding, savouring, gratitude letters and forgiveness letters. |
|
実験的：Positive Cognitive Behavioral Therapy (PCBT)
In this experimental group, the participants will receive an intervention plan based on incorporating positive psychology and solution-focused brief therapy (Bannink & Geschwind, 2021) within the model of cognitive behavioral therapy. |
In this experimental group, the participants will receive an intervention plan based on incorporating positive psychology and solution-focused brief therapy (Bannink & Geschwind, 2021) within the model of cognitive behavioral therapy. The 8-week session plan emphasizes on what is better, exploring the existing resources and self-monitoring to improve wellbeing and quality of life.
他の名前：
|
|
他の：Waitlist Control Group
The participants who will be assigned to this group will be on the waitlist during the active research period. Post-test will be collected at the time as the experimental group to compare the results. After the completion of research data, waitlist participants will be offered and invited to enrol for intervention. |
Participants allocated to this group will be considered as on the waitlist during the active data collection period. This group will serve as a comparison group to see the effectiveness of PPT and PCBT. |
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 |
|---|---|---|
|
Psychological Distress
時間枠：Baseline and 8th Week
|
Depression, Anxiety and Stress Scale DASS-21 is a self-report questionnaire designed to examine three negative emotional states. The scale has 21 items, with 7 items for each subdomain. |
Baseline and 8th Week
|
|
PERMA Profiler
時間枠：Baseline and 8th Week
|
23-item questionnaire for assessing five elements, including positive emotion, engagement, relationships, meaning, accomplishment), along with negative emotion and health. |
Baseline and 8th Week
|
|
Brief Coping Orientation to Problems Experienced Inventory
時間枠：Baseline and 8th Week
|
Self-report 28-item questionnaire to measure coping with sress |
Baseline and 8th Week
|
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 |
|---|---|---|
|
Character Strengths
時間枠：Baseline and 8th week
|
72-item Character Strength Survey to assess 24 universal character strengths. |
Baseline and 8th week
|
協力者と研究者
捜査官
捜査官
- 主任研究者：Mahum Azhaar、Institute of Professional Psychology, Bahria University Karachi
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 (推定)
一次修了
研究の完了 (推定)
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
- No.IPP/ERC/OM/31315/2025
- No.IPP/ERC/OM/31315/2025 (その他の識別子：Institute of Professional Psychology, Bahria University Karachi, Pakistan)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
Due to the nature of the research participants and as per the standard operating procedures (SOPs) for research and mental health sessions inside Sindh prison, the researcher has signed to comit full compilance with prison rules and guidelines to ensure confidentiality and data protection.
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
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。