Online Acceptance and Commitment Therapy-Based Physical Literacy Program for Socioeconomically Disadvantaged Women Living With Overweight
Effects of a Brief Online Acceptance and Commitment Therapy-Based Physical Literacy Program in Socioeconomically Disadvantaged Women Living With Overweight: A Randomized Controlled Trial
This two-group, parallel, individually randomized controlled trial will evaluate a brief, live, online Acceptance and Commitment Therapy (ACT)-based physical literacy program among 60 socioeconomically disadvantaged adult women living with overweight. Participants will be randomized in a 1:1 ratio to either the intervention group or a waitlist control group.
The intervention consists of six weekly approximately 60-minute online group sessions integrating the six ACT processes with adult physical literacy education, guided movement, and graded home-based exercise snacks, followed by an independent-practice week and an approximately 60-minute booster session. Assessments will be conducted at baseline, immediately before the booster following completion of the six core sessions, and at post-booster follow-up. The study will compare changes between the intervention and waitlist control groups over the study period.
調査の概要
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Ayla Rezvan Reha, PhD
- 電話番号:+905340571233
- メール:aylarezvanreha@aydin.edu.tr
研究場所
-
-
Avcilar
-
Istanbul、Avcilar、トルコ(Türkiye)
- 募集
- Online
-
コンタクト:
- Navid Reha, PhD
- 電話番号:+905350223304
- メール:navidrha@yahoo.com
-
-
参加基準
適格基準
就学可能な年齢
- 大人
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Eligibility required: (a) age 18 to 64 years old; (b) residence in Gümüşpala, Avcılar, Istanbul; (c) BMI of 25.0-29.9 kg/m²; (d) annual equivalized net disposable household income below TRY 144,690, the 60%-of-median threshold in the 2025 Turkish Statistical Institute poverty statistics, based on the 2024 income reference period (Turkish Statistical Institute, 2025); (e) no completion of high school (ISCED Levels 0-2; UNESCO Institute for Statistics, 2012); (f) ability to read and understand Turkish; (g) access to a smartphone, WhatsApp, and the internet; (h) willingness to complete all assessments; and (i) written informed consent.
Exclusion Criteria:
- pregnancy or childbirth within the previous six months; a medical or musculoskeletal condition, or professional advice, precluding or substantially restricting physical activity; concurrent participation in another structured weight-management, physical-activity, or psychological intervention; a cognitive or psychiatric condition substantially limiting comprehension or informed consent; or inability to complete study assessments.
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:他の
- 割り当て: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)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
介入なし:キャンセル待ち管理
|
|
|
実験的:ACT-Based Physical Literacy Program
|
Participants receive the live online ACT-based physical literacy program consisting of six weekly approximately 60-minute group sessions, an independent-practice week, and an approximately 60-minute booster session.
|
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 |
時間枠 |
|---|---|
|
Change From Baseline in Physical Literacy Scale for Adults (PLAS) Total Score
時間枠:Baseline, Week 7 (post-core/pre-booster), and Week 11 (4-week post-booster follow-up)
|
Baseline, Week 7 (post-core/pre-booster), and Week 11 (4-week post-booster follow-up)
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
Change From Baseline in PERMA-Profiler Overall Well-Being Score
時間枠:Baseline, Week 7 (post-core/pre-booster), and Week 11 (4-week post-booster follow-up)
|
Baseline, Week 7 (post-core/pre-booster), and Week 11 (4-week post-booster follow-up)
|
|
Change From Baseline in Psy-Flex Scale Score
時間枠:Baseline, Week 7 (post-core/pre-booster), and Week 11 (4-week post-booster follow-up)
|
Baseline, Week 7 (post-core/pre-booster), and Week 11 (4-week post-booster follow-up)
|
|
Change From Baseline in Total Physical Activity Measured by the Global Physical Activity Questionnaire (GPAQ)
時間枠:Baseline, Week 7 (post-core/pre-booster), and Week 11 (4-week post-booster follow-up)
|
Baseline, Week 7 (post-core/pre-booster), and Week 11 (4-week post-booster follow-up)
|
|
Change From Baseline in Body Mass Index (BMI)
時間枠:Baseline, Week 7 (post-core/pre-booster), and Week 11 (4-week post-booster follow-up)
|
Baseline, Week 7 (post-core/pre-booster), and Week 11 (4-week post-booster follow-up)
|
|
Change From Baseline in Waist Circumference
時間枠:Baseline, Week 7 (post-core/pre-booster), and Week 11 (4-week post-booster follow-up)
|
Baseline, Week 7 (post-core/pre-booster), and Week 11 (4-week post-booster follow-up)
|
協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
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
詳しくは
本研究に関する用語
その他の研究ID番号
- 2026/08
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
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。