- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03114709
Mindful Movement for Physical Activity and Wellbeing in Older Adults
Mindful Movement for Physical Activity and Wellbeing in Older Adults: A Community Based Randomized Hybrid Effectiveness-Implementation Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Physical inactivity in the United States has become a critical public health concern for all age groups. With a large segment of the population rapidly aging, there is growing interest in ensuring mid to older age adults (50+) stay active and reduce sedentariness, to decrease their morbidity and mortality risk. While older adults are advised to engage in at least 150 minutes/week of moderate to vigorous physical activity (PA), most do not. Specific theory based behavioral strategies have been shown to positively affect health and activity behaviors. There is also emerging evidence that mindfulness based interventions (MBI) may facilitate PA through increased mind-body awareness and self-regulation. However, research for MBIs and physical activity is currently limited, both in quantity and methodological rigor.
The broad long-term objective is to optimize physical and sedentary activity levels in middle-older age adults through an integrated mindfulness and behavioral approach scalable for broad dissemination. The University of Minnesota (UMN) will work with the YMCA Greater Twin Cities, a community based organization committed to providing accessible resources to "build healthy spirit, mind and body for all" and making healthy aging a priority. To decrease time between discovery and translation, a two-phase hybrid effectiveness-implementation design will be used.
Phase I will address the following: 1) project organization, barrier/facilitator assessment, protocol development, and training; and 2) evaluation of feasibility of project protocols at multiple levels in a randomized pilot study (n=30) of Mindful Movement versus a modified 10 Keys to Health & Wellbeing educational control using transition milestones.
Phase II will address: 1) investigation of the relative effectiveness of Mindful Movement versus control in a full-scale randomized controlled trial (RCT, n=182) using accelerometer based PA at 9 weeks (primary outcome) and at 26 and 52 weeks (secondary outcomes) as well as other secondary measures include sedentary activity, quality of life, exercise self-efficacy and expectations, mindfulness, wellbeing, bodily pain, and adverse events; and 2) RCT interpretation by providing contextual data from participants, staff, and organizational leadership. These will include: enrollment, adherence, follow up, and fidelity rates; and perceptions of barriers/facilitators, relevance, practicality, affordability and acceptability. This information will be used to create a toolkit for implementation at other YMCA sites.
This project is innovative in that it will be among the first to assess MBIs for enhancing older adults' physical activity in community based settings using a design intended to facilitate and accelerate research translation. Through the UMN and YMCA partnership, there is great potential to develop a sustainable and replicable physical activity intervention with meaningful impact and nationwide reach.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Minnesota
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Edina, Minnesota, United States, 55435
- YMCA Southdale
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Minneapolis, Minnesota, United States, 55455
- University of Minnesota
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Saint Paul, Minnesota, United States, 55104
- YMCA Midway
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- ≥ 50 years of age
- Accelerometer wear time ≥10 hours on at least 4 days in a 7 consecutive day period between baselines
- Self-report of <140 minutes of MVPA per week in 3 months prior to baseline AND accelerometer recorded <100 minutes of MVPA between baselines
- Mini-Mental State score ≥ 24
- Independent self-ambulation
- Provides consent and is willing to participate in data collection activities
Exclusion Criteria:
- Pregnancy
- Unwilling or unable to participate in study activities
- Current or upcoming participation in educational programs similar to those under study
- Medical restrictions to increasing Moderate Vigorous Physical Activity (MVPA) AND health care provider does not provide clearance
- Terminal illness
- Contraindications to mindfulness practice
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mindful Movement
8, 90-minute, in-person, group sessions over 8 weeks
|
The program focuses on enhancing individuals' mindfulness capabilities and skills, specifically attention regulation, body awareness, emotional regulation, and shifts in self-perception, by providing opportunities for education, practice, and social support in mindfulness practices and physical activity.
|
|
Active Comparator: 10 Keys to Health & Wellbeing
8, 90-minute, in-person, group sessions over 8 weeks
|
This community-based educational program provides participants useful content focused on general health related topics including common chronic conditions, social support, social participation, cancer screening, immunization and keeping active.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Moderate-Vigorous Physical Activity (MVPA)
Time Frame: Change score: 9 weeks score - baseline score
|
Minutes/week spent in ≥10-min bouts of MVPA
|
Change score: 9 weeks score - baseline score
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of Life-Euroqol 5D (EQ5D)
Time Frame: 0, 9 weeks
|
The EQ5D captures five dimensions of health (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression) over 5 levels (no problem, slight problem, moderate problem, severe problem, unable to perform/extreme problem).
|
0, 9 weeks
|
|
Exercise Self-Efficacy- Self-Efficacy for Exercise (SEE) scale
Time Frame: 0, 9 weeks
|
Individuals are asked to rate their confidence in their ability to exercise.
Confidence ratings range from 0 (not confident) to 10 (very confident).
|
0, 9 weeks
|
|
Exercise Expectations-Outcome Expectations for Exercise-2 (OEE-2) scale
Time Frame: 0, 9 weeks
|
This is a 13-item instrument focused on beliefs about the positive and negative physical and mental health benefits of exercise.
Responses range from 1 (strongly agree) to 5 (strongly disagree).
|
0, 9 weeks
|
|
Mindfulness- Mindful Attention Awareness Scale (MAAS), Frieberg Mindfulness Inventory (FMI)
Time Frame: 0, 9 weeks
|
The MAAS scale is comprised of 15 items measured on a 6-point scale (1=almost always, 6=almost never).
The FMI addresses 14 items with a four-point response scale (1=rarely, 4=almost always).
|
0, 9 weeks
|
|
Wellbeing-8-item Flourishing Scale
Time Frame: 0, 9 weeks
|
This scale assesses perceived success in relationships, self-esteem, and purpose.
|
0, 9 weeks
|
|
Pain-11 box numerical rating scale
Time Frame: 0, 9 weeks
|
An 11-box numerical rating scale (0=no pain, 10=the worst pain possible) will be used for spinal pain, and upper and lower extremities.
|
0, 9 weeks
|
|
Social Connectedness & Assurance
Time Frame: 0, 9 weeks
|
This includes two, eight-item questionnaires with a six-item scale (strongly agree, strongly disagree).
|
0, 9 weeks
|
|
Physical Activity-International Physical Activity Questionnaire (IPAQ)
Time Frame: 0, 9 weeks
|
An adapted, nine-item instrument addressing days/week and minutes/day spent on physical activity in the past 7 days is used to measure physical activity.
|
0, 9 weeks
|
|
Satisfaction
Time Frame: 9 weeks
|
Participants will rate their overall satisfaction (satisfied, completely dissatisfied) with the intervention.
|
9 weeks
|
|
Intervention Barriers
Time Frame: Planning phase, 0, 9 weeks
|
This qualitative, open ended assessment explores barriers to participation in the intervention.
|
Planning phase, 0, 9 weeks
|
|
Intervention Facilitators
Time Frame: Planning phase, 0, 9 weeks
|
This qualitative, open ended assessment explores facilitators to participation in the intervention.
|
Planning phase, 0, 9 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Roni Evans, PhD, University of Minnesota
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 1611S99323-2
- R21AT009110 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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