Improving Physical Activity and Mobility Via Live Online Exercise Sessions for Older Adults

Sponsor
McMaster University (Other)
Overall Status
Completed
CT.gov ID
NCT04627493
Collaborator
(none)
33
1
2
18.2
1.8

Study Details

Study Description

Brief Summary

The COVID-19 pandemic has undoubtedly resulted in an increased level of personal anxiety, reduced access to support services, and as a secondary complication, increased physical inactivity. Older people appear to be at higher risk of several secondary complications and long-term negative health outcomes. These complications include declines in physical health and mobility, social isolation, and worsening mental health. There is strong evidence in older persons that supports the role of exercise and physical activity in: the alleviation of strength and mobility declines, reducing anxiety and depression, and alleviating cognitive declines. Exercise-based intervention trials have also been shown to reduce social isolation and loneliness. This study will compare an online exercise program delivered via Zoom and a waitlist control group in healthy older persons.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Online exercise
N/A

Detailed Description

This study will examine the impacts of an online exercise program in healthy older persons compared to a waitlist control group. Briefly, participants (healthy persons, age 65-80 years old) will participate in an online group exercise program (designed to meet Canada's Physical Activity Guidelines) via Zoom delivered by Registered Kinesiologists and Physiotherapists for a total of 8 weeks. Participants will be randomly assigned to the exercise group or the waitlist control group. Participants' will undergo assessments of physical activity, life-space mobility, nutrition, loneliness, depression, and anxiety at baseline, end of study, and 8-weeks following the end of the intervention.

Study Design

Study Type:
Interventional
Actual Enrollment :
33 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The study will be a randomized parallel-group trialThe study will be a randomized parallel-group trial
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Improving Physical Activity and Mobility, During a Pandemic, Via Live Online Exercise Sessions for Older Persons: a Pilot RCT
Actual Study Start Date :
Nov 1, 2020
Actual Primary Completion Date :
Apr 11, 2022
Actual Study Completion Date :
May 9, 2022

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Waitlist (Control)

Usual care

Experimental: Exercise

Online exercise program

Behavioral: Online exercise
Participants will participate in an online exercise program on Zoom delivered by Registered Kinesiologists and Physiotherapists three times a week.

Outcome Measures

Primary Outcome Measures

  1. Changes in physical activity [Baseline, post intervention, 8-week follow-up]

    7 day steps and activity-related energy expenditure

Secondary Outcome Measures

  1. Change in life-space mobility score [Baseline, post intervention, 8-week follow-up]

    The University of Alabama Life Space Assessment, UA-LSA, will be used to assess participants life-space mobility score. It is a global marker of older adults' physical and community mobility and it has been shown to relate to objectively-measured step counts.

  2. Change in nutrition [Baseline, post intervention, 8-week follow-up]

    The Screen II (Seniors in the Community Risk Evaluation for Eating and Nutrition) will be used to determine whether individuals have a potential nutritional problem or are at risk of developing one and identifies those who need further nutrition assessment and treatment.

  3. Change in feelings of loneliness [Baseline, post intervention, 8-week follow-up]

    The 11-item Revised University of California Los Angeles loneliness scale (R-UCLA) will be used to assess participants' feelings of loneliness.

  4. Change in the Geriatric Depression Scale score [Baseline, post intervention, 8-week follow-up]

    The Geriatric Depression Scale (GDS-15) contains 15 items that measure the intensity of depressive symptoms on a dichotomous scale (yes or no). The total score ranges from 0 to 15. Higher scores indicate higher levels of depressive symptoms.

  5. Change in the Geriatric Anxiety Inventory score [Baseline, post intervention, 8-week follow-up]

    The Geriatric Anxiety Inventory (GAI) contains 20 items that measure the intensity of anxious symptoms on a dichotomous scale (agree or disagree). The total score ranges from 0 to 20. A score of 10 or over is associated with the presence of a generalized anxiety disorder (GAD).

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Exclusion Criteria:
  1. Experience any physical conditions which may prevent them from engaging in moderate-intensity physical activity including using assistive walking devices (e.g. cane or walker), or injuries;

  2. Have a history of neuromuscular conditions or muscle wasting diseases;

  3. Are currently participating in physical activity, ≥150 minutes of moderate-to-vigorous physical activity per week;

  4. Are not eligible to participate in regular physical activity according to the Canadian Society Exercise Physiology Get Active Questionnaire;

  5. Do not have access to the internet at home via a personal smartphone, tablet (e.g., iPad), or computer.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ivor Wynne Centre Hamilton Ontario Canada L8S 4L8

Sponsors and Collaborators

  • McMaster University

Investigators

  • Principal Investigator: Stuart Phillips, Ph.D., McMaster University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Stuart Phillips, Professor, McMaster University
ClinicalTrials.gov Identifier:
NCT04627493
Other Study ID Numbers:
  • 11429
First Posted:
Nov 13, 2020
Last Update Posted:
Jul 25, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Stuart Phillips, Professor, McMaster University

Study Results

No Results Posted as of Jul 25, 2022