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临床试验/NCT05737745
NCT05737745已完成不适用

The Initial Efficacy of FitEx for Endometrial Cancer Survivors: A Pilot Randomized Controlled Trial of a Walking Promotion Program With or Without Yoga

Carilion Clinic2 个研究点 分布在 1 个国家目标入组 111 人开始时间: 2023年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
111
试验地点
2
主要终点
Moderate to Vigorous Physical Activity of Endometrial Cancer Survivors

研究概览

简要总结

The goal of this clinical trial is to compare physical activity outcomes between endometrial cancer survivors randomized to 1 of 3 conditions: 1) usual care, 2) FitEx, 3) FitEx+yoga. Survivors randomized to FitEx groups will recruit ~3 support team members to complete the intervention with them. The main question[s] it aims to answer are:

  • Do FitEx groups undertake more physical activity than the usual care group?
  • Are there differences in quality of life, self-compassion, flourishing, self-efficacy, social support, habit formation, and fruit /vegetable consumption

Participants will:

  • Wear a Fitbit
  • Complete surveys
  • Participate in 30 minute weekly virtual meetings (FitEx groups only)
  • Receive weekly newsletters (FitEx groups only)

详细描述

The purpose of this pilot study is to evaluate the initial efficacy of FitEx, a physical activity tracking and promotion program, and FitEx+yoga for endometrial cancer survivors (ECS), with focus on improvement of moderate-vigorous physical activity (MVPA) at the completion of the 8-week program. Specifically, this project will recruit early stage ECS with obesity to be randomized to 1 of 3 conditions: 1) usual care, 2) FitEx, 3) FitEx+yoga. ECS in either intervention condition will each select ~3 friends or family members to be their support members (minimum 2 and maximum 5). All ECS will receive a Fitbit to track their MVPA. We will then compare secondary ECS outcome measures between intervention and control groups including quality of life, self-compassion, flourishing, self-efficacy, social support, habit formation and fruit/vegetable consumption. Additionally, support team member MVPA (via Fitbit) and secondary outcomes will be compared. We will also explore long-term MPVA and secondary outcomes in all groups at 6 months.

研究设计

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

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with early stage (I-II) endometrial cancer, any histology
  • Received cancer care at Carilion Clinic after 1/1/2010
  • At least 18 years of age
  • Have adequate comprehension (reading and writing) of the English language
  • Have a BMI ≥ 30 kg/m^2 at screening
  • Have stable internet access or access to a smartphone with internet capabilities
  • Meet the requirements of the Physical Activity Readiness Questionnaire(PARQ)
  • Have the capacity to provide informed consent and are willing to provide informed consent
  • SUPPORT TEAM--
  • Were identified by a participant with endometrial cancer as a member of their support system
  • Are at least 18 years of age
  • Have adequate comprehension (reading and writing) of the English language
  • Have stable internet access or access to a smartphone with internet capabilities
  • Meet the requirements of the Physical Activity Readiness Questionnaire (PARQ)
  • Have the capacity to provide informed consent and are willing to provide informed consent

排除标准

  • Recurrent endometrial cancer
  • Meeting physical activity guidelines set forth by the American Cancer Society at screening (greater than 150 minutes/week of moderate physical activity, or greater than 75 minutes/week of vigorous physical activity)
  • SUPPORT TEAM: Have functional limitations requiring a walker, wheelchair, scooter, or other walking aid which limits their capacity to engage in the intervention safely

研究组 & 干预措施

Usual care

No Intervention

Endometrial cancer survivors will receive standard survivorship care including a one-time educational newsletter about survivorship physical activity and nutrition recommendations. Fitbits will be given to track physical activity.

FitEx-ECS

Experimental

Endometrial cancer survivors and their support team members (as a group of one survivor and their team) will complete the FitEx-ECS intervention program, with a focus on walking. Fitbits will be given to track physical activity.

干预措施: Group-dynamics (Behavioral)

FitEx-ECS

Experimental

Endometrial cancer survivors and their support team members (as a group of one survivor and their team) will complete the FitEx-ECS intervention program, with a focus on walking. Fitbits will be given to track physical activity.

干预措施: Self-monitoring (Behavioral)

FitEx-ECS

Experimental

Endometrial cancer survivors and their support team members (as a group of one survivor and their team) will complete the FitEx-ECS intervention program, with a focus on walking. Fitbits will be given to track physical activity.

干预措施: Weekly virtual sessions- Standard (Behavioral)

FitEx-ECS

Experimental

Endometrial cancer survivors and their support team members (as a group of one survivor and their team) will complete the FitEx-ECS intervention program, with a focus on walking. Fitbits will be given to track physical activity.

干预措施: Newsletters- Standard (Behavioral)

FitEx-ECS+ Yoga

Experimental

Endometrial cancer survivors and their support team members (as a group of one survivor and their team) will complete the FitEx-ECS+yoga intervention program, with a focus on postures, breathwork, and mindfulness. Fitbits will be given to track physical activity.

干预措施: Self-monitoring (Behavioral)

FitEx-ECS+ Yoga

Experimental

Endometrial cancer survivors and their support team members (as a group of one survivor and their team) will complete the FitEx-ECS+yoga intervention program, with a focus on postures, breathwork, and mindfulness. Fitbits will be given to track physical activity.

干预措施: Group-dynamics (Behavioral)

FitEx-ECS+ Yoga

Experimental

Endometrial cancer survivors and their support team members (as a group of one survivor and their team) will complete the FitEx-ECS+yoga intervention program, with a focus on postures, breathwork, and mindfulness. Fitbits will be given to track physical activity.

干预措施: Newsletters- Yoga (Behavioral)

FitEx-ECS+ Yoga

Experimental

Endometrial cancer survivors and their support team members (as a group of one survivor and their team) will complete the FitEx-ECS+yoga intervention program, with a focus on postures, breathwork, and mindfulness. Fitbits will be given to track physical activity.

干预措施: Weekly virtual sessions- Yoga (Behavioral)

结局指标

主要结局

Moderate to Vigorous Physical Activity of Endometrial Cancer Survivors

时间窗: Change from baseline to 8 weeks (post-intervention)

Among survivors, compare changes in objective moderate-vigorous physical activity (MVPA) obtained from FitBits (continuous tracking) between intervention groups and usual care (FitEx-ECS vs. control and FitEx-ECS+yoga vs. control)

次要结局

  • Physical Activity Level (Active or Insufficiently Active)- Survivors(Change from baseline to 8 weeks (post-intervention))
  • Moderate to Vigorous Physical Activity of Endometrial Cancer Survivors- Maintenance(Change from 8 weeks to 6 months (post-intervention))
  • Quality of Life- Survivors(Change from baseline to 8 weeks (post-intervention))
  • Quality of Life Maintenance- Survivors(Change from 8 weeks to 6 months (post-intervention))
  • Servings of Daily Fruits and Vegetables Maintenance- Survivors(Change from 8 weeks to 6 months (post-intervention))
  • Servings of Daily Fruits and Vegetables- Survivors(Change from baseline to 8 weeks (post-intervention))
  • Flourishing- Survivors(Change from baseline to 8 weeks (post-intervention))
  • Flourishing Maintenance- Survivors(Change from 8 weeks to 6 months (post-intervention))
  • Yoga Self-Efficacy- Survivors(Change from baseline to 8 weeks (post-intervention))
  • Yoga Self-Efficacy Maintenance- Survivors(Change from 8 weeks to 6 months (post-intervention))
  • Social Support- Survivors(Change from baseline to 8 weeks (post-intervention))
  • Social Support Maintenance- Survivors(Change from 8 weeks to 6 months (post-intervention))
  • Self-compassion- Survivors(Change from baseline to 8 weeks (post-intervention))
  • Self-compassion Maintenance- Survivors(Change from 8 weeks to 6 months (post-intervention))
  • Habit Formation- Survivors(Change from baseline to 8 weeks (post-intervention))
  • Habit Formation Maintenance- Survivors(Change from 8 weeks to 6 months (post-intervention))
  • Physical Activity Level (Active or Insufficiently Active) Maintenance- Survivors(Change from 8 weeks to 6 months (post-intervention))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Shannon Armbruster

Principal Investigator

Carilion Clinic

研究点 (2)

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