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临床试验/NCT07182071
NCT07182071已完成不适用

Feasibility of a 10-Week Physical Activity Program for Mothers of Children With Developmental Disabilities

University of Wisconsin, Madison2 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2025年9月18日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
19
试验地点
2
主要终点
Feasibility: Recruitment Rate

研究概览

简要总结

The purpose of this study is to determine the feasibility and acceptability of a 10-week supervised Physical Activity program for mothers of children with developmental disabilities. 30 participants will be enrolled: 15 into an Intervention group and 15 into a Waitlist Control group.

详细描述

The specific aims of this study are:

  • Aim 1: Determine the feasibility and acceptability of a 10-week supervised resistance training program for mothers of autistic children.
  • Aim 2: Determine the potential health benefits of the 10-week physical activity program on psychological and physical health outcomes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
25 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Be a mother of a child with a diagnosed developmental disability (e.g., autism spectrum disorder, Down syndrome, intellectual disability) ages 4-
  • Be able to engage in moderate-intensity exercise three times per week.
  • Be able to walk independently for at least a quarter of a mile without assistance.
  • Have reliable childcare arrangements during program sessions (please note: childcare will not be provided).
  • Be available and willing to attend scheduled assessments and group sessions throughout the 10-week program.

排除标准

  • Are currently pregnant.
  • Have a physical disability or medical condition that prevents safe participation in physical activity.
  • Are already engaged in physical activity programs more than twice per week.
  • Have diagnosed mental health conditions that may interfere with consistent attendance or the ability to provide informed consent.
  • Are unable to communicate effectively in English.

研究组 & 干预措施

Physical Activity Program

Experimental

This group will enroll in the 10-week program immediately.

干预措施: Physical Activity Program (Behavioral)

Waitlist Control

Active Comparator

This group will enroll and then be offered the 10-week program next year.

干预措施: Waitlist for Physical Activity Program (Behavioral)

结局指标

主要结局

Feasibility: Recruitment Rate

时间窗: through enrollment (up to 12 weeks)

Feasibility: Percent of Sessions Attended

时间窗: up to 12 weeks

Feasibility: Number of Participants Who Complete the study

时间窗: up to 12 weeks

Acceptability: Participant Experiences

时间窗: up to 12 weeks

Measured qualitatively via semi-structured post-intervention interviews, summarized and reported by participant count.

Acceptability: Participant Satisfaction

时间窗: up to 12 weeks

Measured qualitatively via semi-structured post-intervention interviews, summarized and reported by participant count.

Acceptability: Challenges to Participation

时间窗: up to 12 weeks

Measured qualitatively via semi-structured post-intervention interviews, summarized and reported by participant count.

Acceptability: Facilitators to Participation

时间窗: up to 12 weeks

Measured qualitatively via semi-structured post-intervention interviews, summarized and reported by participant count.

次要结局

  • Efficacy: Grip Strength(baseline, week 5, week 10)
  • Efficacy: Number of Push-Ups Participant Completes with Proper Form(baseline, week 5, week 10)
  • Efficacy: Five Times Sit to Stand Test (FTSST)(baseline, week 5, week 10)
  • Efficacy: Percent Body Fat and Lean Mass(baseline, week 5, week 10)
  • Efficacy: Fat Mass and Fat-Free Mass in Kilograms(baseline, week 5, week 10)
  • Generalized Anxiety Disorder-7 (GAD-7)(baseline, week 5, week 10)
  • Perceived Stress Scale (PSS)(baseline, week 5, week 10)
  • Patient Health Questionnaire-8 (PHQ-8)(baseline, week 5, week 10)
  • Penn State Worry Questionnaire (PSWQ)(baseline, week 5, week 10)
  • SF-12 Health Survey(baseline, week 5, week 10)
  • International Physical Activity Questionnaire (IPAQ)(baseline, week 5, week 10)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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