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OpenTrials
Completed

NCT Number: NCT05279989

Healthy Weight and Stress Management Study

Approximately 1 in 10 mid-life (age 35-64) Americans have mobility impairing disabilities. People with mobility impairing disabilities are defined using the World Health Organization criteria: community living adults with mobility impairment (e.g., amputation, spinal cord injury). Women with mobility impairing disabilities often struggle with stress, abdominal fat (measured as waist circumference), lack of muscle tissue (measured as handgrip strength) and high cardiometabolic risk. This study investigates the usefulness, acceptability, and effectiveness of two strategies to reduce stress, improve health habits, reduce abdominal fat and increase muscle tissue in mid-life women with mobility impairments. These strategies involve either gentle stretching and strengthening exercises or watching informative videos.

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Key information

About this study

About 1 in 10 mid-life (age 35-64) Americans have mobility impairing disabilities, steadily increasing due to medical and technological innovations. People with mobility impairing disabilities (PMI) are defined using the World Health Organization criteria, as community living adults with mobility impairment (e.g., amputation, spinal cord injury). Mid-life is a critical time for people to improve their current functioning and enhance healthy aging, by improving emotional health and increasing physical activity (PA). A review showed PA improves emotional and physical health among PMI. PMI have unique challenges to meeting PA guidelines; innovative strategies are needed to achieve emotional and physical benefits for optimal health and aging.

The higher prevalence of daily stress encountered by mid-life PMI is linked to emotional health and abdominal fat (cardiometabolic disease risk) that can lead to premature mortality. This is especially so for women with mobility impairment (WMI) who have higher prevalence of excess body fat, higher cardiometabolic risk, and are not eligible for most interventions that involve PA. PA interventions also increase muscle mass, which helps to prevent cardiometabolic conditions. Although vigorous PA may not be well-suited for WMI, lighter intensity PA such as Tai Chi, Qigong and Yoga-also called meditative movement-adapted for seated practice, are a possible solution.

Tai Chi and Qigong have been tested in non-impaired populations. Our work combines these two forms of low-to-moderate PA meditative movement, Tai Chi and Qigong (TCQ), in a mind-body practice. Our research, and others', show that TCQ consistently shows strong improvement in women in depressive symptoms, anxiety, emotional eating, and sleep quality-all contributing to excess abdominal fat (measured as waist circumference), improved muscle tissue (measured as handgrip strength) and strongly associated with cardiometabolic risk. Conventional health assessment strategies do not always work well for PMI; recent innovations have yielded scalable, low-contact assessment. We have demonstrated robust recruitment, reliable questionnaire administration and strong intervention implementation expertise via social media, video sharing, and gaming platforms.

Aim 1: Assess the potential efficacy of TCQ to reduce waist circumference and increase handgrip strength compared to controls from T1 to T2 and sustain this change to T3 and T4 when compared to control.

Aim 2: Assess the potential efficacy of TCQ to reduce stress-related behaviors (depressive symptoms, anxiety, emotional eating, and sleep) that impact abdominal fat and strength when compared to control.

Aim 3: Evaluate the feasibility and acceptability of an online delivered TCQ intervention in women with mobility impairments.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Community dwelling.
  • Female.
  • Age 35-64.
  • Waist circumference >83 cm (~35 inches).
  • Have a self-reported mobility impairment due to a chronic (>1 year).
  • Physically disabling condition (regularly using an assistive device).
  • Access to an email address and a working phone, mobile device, or personal computer or device with a high-speed internet connection.
  • Understand spoken and written English and be willing to be randomized.
  • Willing to engage in the intervention for 12 weeks, be available for two Zoom calls for data collection at T1, T2, T3, and T4 (Week 1, Week 4, Week 8, and Week 12).

Exclusion criteria

  • People with full mobility.
  • People who have been regularly practicing (e.g., ≥2 or more times per month for the past 6 months) any form of meditative movement including, but not limited to, Yoga, Tai Chi or Qigong.
  • Pregnant, lactating, or planning to become pregnant in the next 6 months,
  • Participants outside of the age range will be excluded from participation.
  • Adults unable to consent and prisoners will be excluded.

Treatment and study plan

Seated Tai Chi Qigong

Other

Participants will receive seated Tai Chi Qigong videos.

Health Information Videos

Other

Participants will receive videos of health information.

Primary outcomes

  1. Waist Circumference assessed by measuring tape

    Time frame: Baseline

    Waist Circumference assessed by measuring tape

  2. Waist Circumference assessed by measuring tape

    Time frame: Week 4

    Waist Circumference (cm) assessed by measuring tape

  3. Waist Circumference measured by measuring tape

    Time frame: Week 8

    Waist Circumference (cm) assessed by measuring tape

  4. Waist Circumference measured by measuring tape

    Time frame: Week 12

    Waist Circumference (cm) assessed by measuring tape

  5. Handgrip strength measured by isokinetic handgrip dynamometry

    Time frame: Baseline

    Weight (kg) resisted measured by handgrip dynamometer

  6. Handgrip strength measured by isokinetic handgrip dynamometry

    Time frame: Week 4

    Weight (kg) resisted measured by handgrip dynamometer

  7. Handgrip strength measured by isokinetic handgrip dynamometry

    Time frame: Week 8

    Weight (kg) resisted measured by handgrip dynamometer

  8. Handgrip strength measured by isokinetic handgrip dynamometry

    Time frame: Week 12

    Weight (kg) resisted measured by handgrip dynamometer

  9. Depressive Symptoms assessed by Center for Epidemiologic Studies Depression Scale

    Time frame: Baseline

    Center for Epidemiologic Studies Depression Score ranging from 0-3, with lower scores indicating a more desirable outcome.

  10. Depressive Symptoms assessed by Center for Epidemiologic Studies Depression Scale

    Time frame: Week 12

    Center for Epidemiologic Studies Depression Score ranging from 0-3, with lower scores indicating a more desirable outcome.

  11. Anxiety assessed by Generalized Anxiety Disorder 7-item Scale

    Time frame: Baseline

    Generalized Anxiety Disorder 7-item Scale Score ranging from 0-21, with lower scores indicating a more desirable outcome.

  12. Anxiety assessed by Generalized Anxiety Disorder 7-item Scale

    Time frame: Week 12

    Generalized Anxiety Disorder 7-item Scale Score ranging from 0-21, with lower scores indicating a more desirable outcome

Secondary outcomes

  1. Emotional Eating assessed by Mindful Eating Questionnaire - 5 Factor

    Time frame: Baseline

    Mindful Eating Questionnaire - 5 Factor Score scored on a scale of 1-4, with higher scores signifies more mindful eating

  2. Emotional Eating assessed by Mindful Eating Questionnaire - 5 Factor

    Time frame: Week 12

    Mindful Eating Questionnaire - 5 Factor Score scored on a scale of 1-4, with higher scores signifies more mindful eating

  3. Sleep Quality assessed by the Pittsburgh Sleep Quality Index

    Time frame: Baseline

    Pittsburgh Sleep Quality Index Score, scored on a scale of 0-21, with higher scores indicating poorer sleep quality

  4. Sleep Quality assessed by Pittsburgh Sleep Quality Index

    Time frame: Week 4

    Pittsburgh Sleep Quality Index Score, scored on a scale of 0-21, with higher scores indicating poorer sleep quality

  5. Sleep Quality assessed by Pittsburgh Sleep Quality Index

    Time frame: Week 8

    Pittsburgh Sleep Quality Index Score, scored on a scale of 0-21, with higher scores indicating poorer sleep quality

  6. Sleep Quality assessed by Pittsburgh Sleep Quality Index

    Time frame: Week 12

    Pittsburgh Sleep Quality Index Score, scored on a scale of 0-21, with higher scores indicating poorer sleep quality

  7. Food Consumption Frequency assessed by the Dietary Screener Questionnaire

    Time frame: Baseline

    Dietary Screener Questionnaire responses measuring food consumption frequency

  8. Food Consumption Frequency assessed by the Dietary Screener Questionnaire

    Time frame: Week 12

    Dietary Screener Questionnaire responses measuring food consumption frequency

  9. Physical Functioning assessed by the Short-Form Health Survey

    Time frame: Baseline

    The Short-Form Health Survey Score scored 0-100, with higher scores indicating greater physical function

  10. Physical Functioning assessed by The Short-Form Health Survey

    Time frame: Week 12

    The Short-Form Health Survey Score scored 0-100, with higher scores indicating greater physical function

  11. Well-Being assessed by the Short-Form Health Survey

    Time frame: Baseline

    The Short-Form Health Survey Score scored 0-100, with higher scores indicating greater well-being

  12. Well-Being assessed by the Short-Form Health Survey

    Time frame: Week 12

    The Short-Form Health Survey Score scored 0-100, with higher scores indicating greater well-being

Sponsors and collaborators

Lead sponsor

Arizona State University

Other

Registry information

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Mar 15, 2022
Registry last updated
Feb 2, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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