Mayo Posture Positivity Power Program for Active and Aging Individuals in Communities

December 21, 2021 updated by: Takashi Nagai, Mayo Clinic

Mayo Posture Positivity Power Program (MayoP4) for Active and Aging Individuals in Communities

The research is designed to answer effectiveness of community-based multimodal intervention programs on physical, mental, cognitive, social, and environmental in active and aging individuals.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Despite that musculoskeletal diseases/conditions are the leading cause of disability and frailty/mortality in aging individuals, the musculoskeletal health is given little consideration. Exercise is essential and effective publicly-available medicine for management/prevention of obesity, lack of physical activity, chronic disease, frailty, and mental stress/anxiety/depression without any side-effects from drug use/abuse.

More recently, multimodal interventions with physical, postural, mindfulness, and power exercises have shown to be effective improving both physical and mental health. To expand the recent trend in multimodal intervention, the current proposal will examine effects of community-based multimodal intervention on physical, psychological, cognitive, social, and environmental characteristics in aging individuals. Simultaneously, a cross-sectional study will establish normative values and inter-relationships.

One simple (15 minutes a day /2-3 times a week) yet comprehensive multimodal (balance, posture/thoracic spine, hopping, and mindfulness) intervention could provide a practical solution for aging individuals. Such a program could be implemented individually or by community staff, which would allow for a large-scale community implementation.

Therefore, the overall objective of the project is to explore effects of a community-based, simple, multimodal intervention program (MayoP4) for aging individuals. A small group intervention with friends and club/family members will help peer-to-peer support/team spirit and improve positive engagement.

The secondary objective of this project is to establish normative values and examine interrelations among various frailty/mortality risk factors. In addition to physical activity, musculoskeletal, balance/posture, and psychological/wellness factors, there are many additional elements associated with frailty/mortality risk. These include, but are not limited to, positive thinking/behavior (optimism), sufficient sleep, and cognitive/social/environmental considerations. Physical frailty plays an important role and positively influences all other domains; however, this relationship among aging individuals in our communities remains to be established.

Study Type

Interventional

Enrollment (Actual)

59

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Minnesota
      • Rochester, Minnesota, United States, 55905
        • Mayo Clinic

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

65 years and older (OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Participants must be physically capable (defined as easy to moderate physical activities daily at least 60 minutes).
  • Participants also must have a normal (18.5-24.9kg/m2) or overweight BMI (25-29.9kg/m2).
  • Participants must be able to speak, listen, read, and understand sentences written in English.

Exclusion Criteria:

  • Participants who display more than two risk factors for coronary artery disease
  • Participants who have a history of falls, osteoporosis, osteoarthritis, or orthopedic or neurological conditions (i.e., stroke)
  • Participants who take medications that cause dizziness or slow movement
  • Participants who smoke
  • Participants who have a body mass to height squared ratio greater than 30kg/m2 or less than 18.4kg/m2, blood pressure greater than 140/90 mmHg, or a history of heart conditions.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: NON_RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
NO_INTERVENTION: Control Group
No intervention
EXPERIMENTAL: MayoP4 Group
MayoP4 is a 15-minute warmup with 4 different components of exercise: balance, posture, hopping/jumping, and movement-based mindfulness.
MayoP4 is a 15-minute warmup with 4 different components of exercise: balance, posture, jumping/hopping, and movement-based mindfulness.
Other Names:
  • MayoP4

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline demographic information at 12 weeks
Time Frame: baseline, 12 weeks
  • Age (continuous),
  • Race (White, Black, Asian, Pacific Islander, Hispanic/Latino, American Indian)
  • Marital Status (married, divorced/separated/single, widowed)
  • Education (less than High School, High School, College, Graduate School)
  • Height
  • Weight
  • Smoking (never, former, current)
  • Alcohol (intake from wine, beer, and liquor - none, 1-14g/day, >15g/day.)
  • For Women Only: Women health questions will be asked for past/present conditions (pregnancy, hormonal treatment, menopause, supplements, medications, etc.)
baseline, 12 weeks
Change from baseline frailty index information at 12 weeks, 1
Time Frame: baseline, 12 weeks
• Comprehensive Frailty Assessment Instrument Plus: Assessment of frailty in physical, psychological, social, cognitive, and environmental domains
baseline, 12 weeks
Change from baseline Knee/Osteoarthritis Self-Reported Questionnaires at 12 weeks, 1
Time Frame: baseline, 12 weeks
• International Knee Documentation Committee Subjective Knee Evaluation
baseline, 12 weeks
Changes from baseline psychological assessment at 12 weeks, 1
Time Frame: baseline, 12 weeks
• Perceived Stress Scale: A 14-item self-report tool that provides a global measure of perceived stress
baseline, 12 weeks
Changes from baseline overall health surveys / physical frailty test at 12 weeks, 1
Time Frame: baseline, 12 weeks
• Medical Outcomes Study 36-Item Short-Form Health Survey: A common medical questionnaire for general health and wellbeing
baseline, 12 weeks
Changes from baseline hand-Grip Strength at 12 weeks
Time Frame: baseline, 12 weeks
A standard handgrip isometric strength test performed using a Jamar Hydraulic Hand Dynamometer.
baseline, 12 weeks
Changes from baseline walking speed at 12 weeks
Time Frame: baseline, 12 weeks
you will be asked to walk as fast as you can for 4-meter (12 feet) three times. 4-meter distance will be marked with a tape.
baseline, 12 weeks
Changes from baseline knee strength at 12 weeks
Time Frame: baseline, 12 weeks
A custom-built knee strength measuring device will examine your quadriceps muscles (front muscles of the thigh) and hamstrings muscles (back muscles of the thigh).
baseline, 12 weeks
Changes from baseline knee muscular steadiness at 12 weeks
Time Frame: baseline, 12 weeks
• Force steadiness test will assess individual's ability to hold their muscular force for 10 seconds steady.
baseline, 12 weeks
Changes from baseline balance at 12 weeks
Time Frame: baseline, 12 weeks
Standing balance with eyes-open and eyes-closed will be tested.
baseline, 12 weeks
Changes from baseline posture at 12 weeks
Time Frame: baseline, 12 weeks
standard 2D camera will be used to assess standing posture and overhead squatting posture.
baseline, 12 weeks
Changes from baseline heel bone ultrasound scan at 12 weeks
Time Frame: baseline, 12 weeks
Quantitative ultrasound is accurate, inexpensive, and portable alternative to DXA bone mineral density. This device will measure the speed of sound and the frequency-dependent attenuation of the sound waves to calculate the stiffness index which is equivalent to bone mineral density.
baseline, 12 weeks
Changes from baseline ultrasound-based bilateral anterior thigh thickness at 12 weeks
Time Frame: baseline, 12 weeks
A diagnostic musculoskeletal ultrasound will be used to measure your thigh muscle size.
baseline, 12 weeks
Changes from baseline frailty index at 12 weeks, 2
Time Frame: baseline, 12 weeks
• A multi-domain frailty assessment
baseline, 12 weeks
Changes from baseline knee/osteoarthritis self-reported questionnaires at 12 weeks, 2
Time Frame: baseline, 12 weeks
• Knee Osteoarthritis Outcome Score
baseline, 12 weeks
Changes from baseline knee/osteoarthritis self-reported questionnaires at 12 weeks, 3
Time Frame: baseline, 12 weeks
• Knee Outcome Survey-Activities of Daily Living
baseline, 12 weeks
Changes from baseline knee/osteoarthritis self-reported questionnaires at 12 weeks, 4
Time Frame: baseline, 12 weeks
• Global Rating score
baseline, 12 weeks
Changes from baseline psychological assessment at 12 weeks, 2
Time Frame: baseline, 12 weeks
• Generalized Anxiety Disorder 7-item: A 7-item questionnaire which asks how often, during the last 2 weeks, the participant was bothered by anxiety-related symptoms
baseline, 12 weeks
Changes from baseline psychological assessment at 12 weeks, 3
Time Frame: baseline, 12 weeks
• Mindfulness Attention Awareness Scale: A 15-item measure assessing mindfulness of moment to moment experience
baseline, 12 weeks
Changes from baseline psychological assessment at 12 weeks, 4
Time Frame: baseline, 12 weeks
• Patient Health Questionnaire-9: A self-administered tool for assessing depression
baseline, 12 weeks
Changes from baseline psychological assessment at 12 weeks, 5
Time Frame: baseline, 12 weeks
• Optimism. Revised Life Orientation Test: A questionnaire to assess individual's optimism and related to healthy aging seniors
baseline, 12 weeks
Changes from baseline overall health surveys / physical frailty test at 12 weeks, 2
Time Frame: baseline, 12 weeks
• Barthel Index of Activities of Daily Living: A 10-item questionnaire for activities of daily living
baseline, 12 weeks
Changes from baseline overall health surveys / physical frailty test at 12 weeks, 3
Time Frame: baseline, 12 weeks
• Pittsburgh Sleep Quality Index: A self-reported questionnaire that assesses sleep quality and disturbances
baseline, 12 weeks
Changes from baseline overall health surveys / physical frailty test at 12 weeks, 4
Time Frame: baseline, 12 weeks
• Sarcopenia Questionnaire: This questionnaire will ask participants basic physical capability
baseline, 12 weeks
Changes from baseline overall health surveys / physical frailty test at 12 weeks, 5
Time Frame: baseline, 12 weeks
• Mini Nutritional Assessment - Short Form: Assesses malnutrition, weight loss, and a lack of appetite
baseline, 12 weeks
Knee Flexion and Extension Visual-Motor Reaction Time
Time Frame: baseline, after 12 weeks
Subjects will be asked to kick up (quadriceps - knee extensors) or pull back (hamstrings - knee flexors) as soon as an arrow is displaced up or down, respectively.
baseline, after 12 weeks
Changes from baseline ultrasound-based bilateral anterior thigh muscle stiffness measurements at 12 weeks
Time Frame: baseline, 12 weeks
Ultrasound probe will be placed at the mid-thigh (the quadriceps) during rest and knee extension strength force steadiness testing.
baseline, 12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Takashi Nagai, PhD, Mayo Clinic

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

December 14, 2020

Primary Completion (ACTUAL)

June 1, 2021

Study Completion (ACTUAL)

June 1, 2021

Study Registration Dates

First Submitted

October 21, 2020

First Submitted That Met QC Criteria

December 18, 2020

First Posted (ACTUAL)

December 23, 2020

Study Record Updates

Last Update Posted (ACTUAL)

December 22, 2021

Last Update Submitted That Met QC Criteria

December 21, 2021

Last Verified

December 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • 20-001520

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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