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Mindfulness Audio Recordings for Postmenopausal Women
N/A
Waitlist Available
Led By Emma Fortune-Ngufor, PhD
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 weeks
Awards & highlights
Study Summary
This trial looks at how postmenopausal women respond to a mindfulness audio recording when combined with physical activity, to see if it helps them be more active.
Who is the study for?
This trial is for postmenopausal women who can walk without aid, own a smartphone or tablet, are over one year postmenopausal, and consider themselves underactive. It's not for those needing walking aids, unable to use smart devices, cannot consent independently, swim as primary exercise (monitors aren't waterproof), or are less than one year postmenopausal.Check my eligibility
What is being tested?
The study tests if mindfulness audio recordings can be an acceptable tool for increasing daily physical activity in postmenopausal women. Participants will use these recordings alongside their regular activities to see if it helps them become more active.See study design
What are the potential side effects?
Since the intervention involves only mindfulness audio recordings used with physical activity, there are no direct medical side effects expected from the recordings themselves. However, increased physical activity may lead to typical exertion-related discomforts.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Acceptability of a mindfulness-based physical activity intervention
Secondary outcome measures
Daily physical activity
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Group A/InterventionExperimental Treatment1 Intervention
Subjects will use mindfulness audio recordings along with their physical activity, and will receive a weekly health coaching phone call along with supplemental educational materials.
Group II: Group B/ControlActive Control1 Intervention
Subjects will receive education materials on healthy habits for increasing physical activity based on the National Institutes of Health, and bi-weekly check-in phone call.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Mindfulness Audio Recordings
2022
N/A
~30
Find a Location
Who is running the clinical trial?
Mayo ClinicLead Sponsor
3,206 Previous Clinical Trials
3,767,060 Total Patients Enrolled
3 Trials studying Postmenopausal
145 Patients Enrolled for Postmenopausal
Emma Fortune-Ngufor, PhDPrincipal InvestigatorMayo Clinic
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You cannot swim as your primary form of exercise because the activity monitors are not waterproof.You are not able or do not want to keep track of your daily activities.You do not engage in regular physical activity.
Research Study Groups:
This trial has the following groups:- Group 1: Group A/Intervention
- Group 2: Group B/Control
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is this investigation currently admitting participants?
"According to the information published on clinicaltrials.gov, this medical trial has ceased recruitment for now; its initial post-date being November 1st 2022 and latest edit occurring October 19th 2022. Nevertheless, 15 other trials are actively seeking participants at present."
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