Cultural Adaptation of an Online Parenting Intervention to Reduce the Risk of Depression and Anxiety in Adolescents (PiP_ Pakistan)
2026年8月25日 更新者：Pakistan Institute of Living and Learning
Cultural Adaptation and Randomized Controlled Trial Evaluation of an Online Parenting Intervention to Reduce the Risk of Depression and Anxiety in Adolescents
Depression and anxiety are common mental health problems among adolescents and can affect their relationships, education, physical health and everyday lives.
In Pakistan, many adolescents experience emotional difficulties, but mental health problems are often overlooked.
Stigma, limited awareness about mental health and difficulties accessing professional support can prevent young people and families from getting the help they need.
Parents play an important role in supporting their adolescents' mental health.
The way parents communicate with their children, set family rules, manage conflict, provide emotional support and encourage healthy habits can influence adolescents' wellbeing.
However, parenting programmes that help parents reduce the risk of depression and anxiety in adolescents are limited in Pakistan.
This study aims to address this gap by adapting and evaluating an online parenting programme called Partners in Parenting (PiP) for families in Pakistan.
Hence, the aim is to find out whether the culturally adapted PiP programme can reduce the risk of depression and anxiety among adolescents and improve parenting practices and parent-adolescent relationships.
We will also explore whether the programme is acceptable, easy to use and helpful for Pakistani families, and whether it provides good value for the resources required to deliver it.
First, we will work with adolescents, parents, grandparents, teachers and health professionals to understand their experiences and views about adolescent mental health and parenting in Pakistan.
Their feedback will be used to make PiP culturally appropriate and relevant to Pakistani families.
People with lived experience of adolescent mental health difficulties will also be involved throughout the adaptation process.
The study will then evaluate the adapted programme with 1,300 parent-adolescent pairs across eight cities in Pakistan: Karachi, Hyderabad, Lahore, Rawalpindi, Multan, Qambar Shahdad Kot, Larkana and Sukkur.
Families will be randomly allocated to three groups i.e partners in parenting, Shamiri, and control group.
PiP is an online programme designed to help parents develop positive parenting skills and strengthen their relationships with their adolescents.
Adolescents participating in the study will receive a four-session programme called Shamiri, which focuses on developing a growth mindset, gratitude and personal values.
Process evaluation will explore how the programme is delivered and experienced in real-world settings.
This will help us understand whether families engage with and complete the programme, which parts they find useful or difficult, how acceptable and practical the intervention is, and what factors may support or prevent successful implementation.
We will gather information from parents, adolescents and those involved in delivering or supporting the programme to understand their experiences and identify ways the programme could be improved and implemented more effectively.
The findings could help identify practical and accessible ways to support adolescent mental health in Pakistan.
The study will give parents and adolescents an opportunity to contribute to research that aims to improve mental health support for young people in Pakistan.
調査の概要
詳細な説明
Research Aim: To test the preliminary efficacy of PiP intervention in reducing the risk of depression in adolescents at end of intervention (3-months) using the adolescent-report Short Mood and Feelings Questionnaire- SMFQ which assesses depressive symptoms in children and adolescents. Methods: Methods:
Work Package 1- Understanding local context to co-design PiP intervention. A qualitative approach will be used to conduct in-depth interviews with adolescents with lived experience of mental health difficulties, their parents and grandparents, health professionals (mental health experts/ family physicians) and teachers (15-20 participants/category) to explore the mental health difficulties experiences of adolescents, parenting and how stakeholders think parents should support adolescents to adapt PiP modules. The Lived Experience Experts (LEE) groups will be developed province wise who will be actively engaged in the adaptation process of the intervention. Work Package 2-Randomized Controlled Trial of culturally adapted PiP intervention compared to control arm. This is a three-arm, parallel group design RCT, comparing intervention to the control arm. Parents who have an adolescent aged 12-18 years, Have sufficient internet literacy, access, and/or ability to read and write, will be invited to participate. A total 1300 participants will be approached in schools, colleges and community settings in 8 cities in Pakistan: Karachi, Hyderabad, Lahore, Rawalpindi, Multan, Qamabar Shahdad Kot, Larkana, and Sukker. Work Package 3: Process evaluation underpinned by Interpretative phenomenological analysis. This WP involves semi-structured interviews (n=15/category) with adolescents and their parents from the intervention arm and research team to explore their experiences of engaging in the intervention and their views on its cultural appropriateness in empowering them to support adolescent mental health, reduce depression and anxiety amongst adolescents and improve parenting relationships. Only research team members directly involved in the implementation or delivery of the intervention will be eligible to participate in the semi-structured interviews.
研究の種類
介入
入学 (推定)
1300
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
- 名前：Rabia Sattar, PhD (Scholar)
- 電話番号：+923332976807
- メール：rabia.sattar@pill.org.pk
研究連絡先のバックアップ
- 名前：Nasim Chaudhry, MD
- 電話番号：+923160129255
- メール：nasim.chaudhry@pill.org.pk
研究場所
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Sindh
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Karachi、Sindh、パキスタン、75600
- Pakistan Institute of Living and Learning
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コンタクト：
- Nasim Chaudhry, MD
- 電話番号：0922135371084
- メール：nasim.chaudhry@pill.org.pk
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コンタクト：
- Rabia Sattar, PhD Scholar
- 電話番号：+92 3332976807
- メール：rabia.sattar@pill.org.pk
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
健康ボランティアの受け入れ
はい
説明
Inclusion Criteria
- Parents who have an adolescent aged 12-18 years. (If they have more than one child in this age bracket, only one child can participate that will be depend on their own willingness and mutual understanding).
- Have sufficient internet literacy, access, and/or ability to read and write.
- Only 1 parent-adolescent dyad/family will be eligible to participate, that will be depend on their own willingness and mutual understanding.
Exclusion Criteria
- Presence of a diagnosed severe psychiatric disorder (e.g., bipolar disorder or Schizophrenia) or a severe physical illness in either the parent or adolescent that would significantly impair their ability to participate meaningfully in the study procedures.
- Lack of capacity to provide informed consent (parent) or assent (adolescent), as determined by the trained research team.
- Families who are temporary residents in the study city
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
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：防止
- 割り当て：ランダム化
- 介入モデル：階乗代入
- マスキング：独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的：Partners in Parenting
The Partners in Parenting (PiP) intervention is a fully automated, web-based parenting program.
Nine modules are available in total, and parents can further tailor their program by selecting additional modules not initially recommended or opting out of recommended ones.
Modules feature interactive activities, goal-setting exercises, audio clips, vignettes, illustrations, and an end-of-module quiz with immediate feedback to reinforce learning.
Each module takes approximately 15-25 minutes to complete, with one module released weekly to allow time for completion and practice of weekly goals.
Automated weekly emails notify parents when the next module is available via their personalized dashboard.
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The Partners in Parenting (PiP) intervention is a fully automated, web-based parenting program comprising three components.
First, parents complete a self-assessment scale, the Parenting to Reduce Adolescent Depression and Anxiety Scale (PRADAS), which evaluates their current parenting practices against established Guidelines.
Second, based on PRADAS responses, parents receive an individually tailored feedback report highlighting their parenting strengths and areas for improvement.
The feedback is designed to be concise, encourage behavior change, provide practical parenting strategies, and include links to additional resources if desired.
Third, parents are recommended a series of interactive online modules, personalized according to their PRADAS responses.
Nine modules are available in total, and parents can further tailor their program by selecting additional modules not initially recommended or opting out of recommended ones.
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実験的：Shamiri
The Shamiri intervention (from the Swahili word for "thrive") is an evidence-based, 4-week, group-based mental health program designed for adolescents to reduce depression and anxiety.
This intervention is derived from the Growth Mindset Single Session Intervention (GM-SSI) which has demonstrated effectiveness for a range of psychological problems of adolescents, including depression and anxiety
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group-based mental health program designed for adolescents to reduce depression and anxiety.
This intervention is derived from the Growth Mindset Single Session Intervention (GM-SSI) which has demonstrated effectiveness for a range of psychological problems of adolescents, including depression and anxiety, as well as other distress-related difficulties.
Evidence indicates that GM-SSI can serve as a low-cost approach to enhance youth resilience and mental health.
The shamiri is mindset program comprising: a growth mindset module (2 sessions), a gratitude module (1 session), and a values affirmation module (1 session).
Sessions are delivered weekly, each lasting approximately one hour.
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介入なし：Control
Parents and adolescents in the control group will be assessed at baseline and 3rd month outcome assessment.
To ensure equitable access to intervention materials for participants in the control group, they will have access to these materials after the follow-up assessments are completed.
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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
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Short Mood and Feelings Questionnaire- SMFQ (Angold et al., 1995)
時間枠：Baseline and 3 months
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The SMFQ, Adolescent-reported, consists of a series of 13 descriptive phrases regarding how the subject has been feeling or acting recently.
It is a screening tool for depression in children and young people aged 6 to 19.
A total score on the child version of the SMFQ of 8 or more is considered significant.
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Baseline and 3 months
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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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Spence Children's Anxiety Scale- (SCAS) Adolescent-report (Spence, 1997):
時間枠：Baseline and 3 months Follow up
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The Spence Children's Anxiety Scale is developed to assess the severity of anxiety symptoms broadly in line with the dimensions of anxiety disorder proposed by the DSM-IV.
The scale assesses six domains of anxiety including generalized anxiety, panic/agoraphobia, social phobia, separation anxiety, obsessive compulsive disorder and physical injury fears.
The scale normally takes around 10 minutes to answer the questions.
Each symptom is rated using a four-point frequency scale indicating how often it is experienced.
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Baseline and 3 months Follow up
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Parenting to Reduce Adolescent Depression and Anxiety Scale (PRADAS) (Cardamone-Breen, Jorm, Lawrence, Mackinnon, & Yap, 2017):
時間枠：Baseline and 3 months
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PRADAS is designed to assess the change in parenting risk and protective factors to reduce risk of depression and anxiety in adolescents.
PRADA assess parenting practices in concordance with the nine domains of PiP current parenting practices against specific recommendations in the Guidelines.
Items are assessed using Likert-type scales and scored as either concordant (1) or non-concordant (0) with the Guidelines' recommendations.
The total score therefore ranges from 0 to 43, with higher scores indicating greater concordance.
Both Adolescent and parent-report assessment will be completed.
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Baseline and 3 months
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The McMaster Family Assessment Device-General Functioning subscale (FAD-GF) (Epstein, Baldwin, & Bishop, 1983):
時間枠：Baseline and 3 months
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The FAD-GF is a brief self-report measure derived from the 60-item Family Assessment Device and can be completed by family members aged 12 years and older with responses rated on a 4-point Likert scale from strongly agree to strongly disagree.
It consists of 12 items assessing overall family functioning, with six positively worded and six negatively worded items, and has been shown to correlate strongly with most FAD subscales, supporting its use as a valid proxy for the full instrument.
The FAD will be administered to both adolescents and parent.
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Baseline and 3 months
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EuroQol 5 Dimensions (Brooks & Group, 2017)
時間枠：Baseline and 3 months
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Health-related quality of life will be assessed using the EQ-5D by exploring 5 areas: mobility, self-care, usual activities, pain/discomfort and anxiety/depression.
Each dimension is rated using the following categories: no problems, slight problems, moderate problems, severe problems, and extreme problems.
In addition, a visual analogue scale (VAS) is included to record the patient's self-rated health.
This scale has been used in previous trials in Pakistan (Alvi et al., 2022; Husain et al., 2021).
The ED 5D will be administered to adolescent.
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Baseline and 3 months
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Client Service Receipt Inventory (CSRI) (Beecham & Knapp, 2001)
時間枠：Baselines and 3 months
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Information on participants' use of both formal and informal (such as Imams/faith healers) health services was collected at baseline and follow-up assessments using a structured form.
The healthcare costs, including staffing, equipment, training, delivering and monitoring, as well as patient-level direct and indirect costs will be collected using the bespoke tool (Alvi et al., 2022).
The CSRI will be administered to adolescent.
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Baselines and 3 months
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Short Mood and Feelings Questionnaire (SMFQ) - (Angold et al., 1995)
時間枠：Baseline and 3 months
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The Mood and Feelings Questionnaire (Short Version) - Parent Report (SMFQ-Parent) is a 13-item measure assessing recent depressive symptomatology in children and adolescents.
The SMFQ-Parent consists of items scored 0 (not true), 1 (sometimes), or 2 (true), reflecting the frequency of depressive symptoms observed in the child over the past two weeks.
The sum of responses to all items produces a total score ranging from 0 to 26.
Higher scores indicate greater severity of depressive symptoms.
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Baseline and 3 months
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The Spence Children's Anxiety Scale - Parent Version (SCAS-Parent) (Nauta et al., 2004):
時間枠：Baseline and 3 months
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SCAS-Parent is a 39-item parent report measure designed to assess anxiety symptoms in children and adolescents across six domains of anxiety (details are provided in SCAS- Adolescents report).
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Baseline and 3 months
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System Usability Scale (SUS) (Bangor, Kortum, & Miller, 2008):
時間枠：Baseline and 3 months
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Usability of the interventions will be measured with SUS.
The SUS is composed of 10 statements that are scored on a 5-point scale of extent of agreement (score 0 to 100).
The reliability is good (α=0.91).
Interventions with scores of 70 and above are accepted as highly usable and scores between 50 and 70 indicate acceptable usability of an intervention.
Interventions with scores 50 and below are subject to concerns about their usability by the target population.
The SUS will be administered to parents.
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Baseline and 3 months
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協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (推定)
2026年9月7日
一次修了 (推定)
2027年9月30日
研究の完了 (推定)
2027年9月30日
試験登録日
最初に提出
2026年8月25日
QC基準を満たした最初の提出物
2026年8月25日
最初の投稿 (実際)
2026年8月27日
学習記録の更新
投稿された最後の更新 (実際)
2026年8月27日
QC基準を満たした最後の更新が送信されました
2026年8月25日
最終確認日
2026年8月1日
詳しくは
本研究に関する用語
その他の研究ID番号
- Partners in Parenting_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?
はい
IPD プランの説明
Only anonymized data will be shared.
Requests to be made to Principal Investigator
IPD 共有時間枠
Once the trial results are published
IPD 共有アクセス基準
Requests should be made to Principal Investigator
IPD 共有サポート情報タイプ
- STUDY_PROTOCOL
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米国FDA規制医薬品の研究
いいえ
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いいえ
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