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Online Acceptance and Commitment Therapy-Based Physical Literacy Program for Socioeconomically Disadvantaged Women Living With Overweight

2026年9月9日 更新者:Navid Reha

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.

研究概览

研究类型

介入性

注册 (估计的)

60

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人

接受健康志愿者

是的

描述

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.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:其他
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
无干预:候补名单控制
实验性的: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.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Change From Baseline in Physical Literacy Scale for Adults (PLAS) Total Score
大体时间: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)

次要结果测量

结果测量
大体时间
Change From Baseline in PERMA-Profiler Overall Well-Being Score
大体时间: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
大体时间: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)
大体时间: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)
大体时间: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
大体时间: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)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月10日

初级完成 (估计的)

2026年12月10日

研究完成 (估计的)

2026年12月10日

研究注册日期

首次提交

2026年9月9日

首先提交符合 QC 标准的

2026年9月9日

首次发布 (实际的)

2026年9月14日

研究记录更新

最后更新发布 (实际的)

2026年9月14日

上次提交的符合 QC 标准的更新

2026年9月9日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • 2026/08

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

Individual participant data are not planned to be shared.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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