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

Aging Clinical Trial

Official title:

Improving Physical Activity and Mobility, During a Pandemic, Via Live Online Exercise Sessions for Older Persons: a Pilot RCT

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04627493
• Other study ID #: 11429
• Status: Completed
• Phase: N/A
• Start date: November 1, 2020
• Est. completion date: May 9, 2022

Study information

• Verified date: September 2023
• Source: McMaster University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 33
• Est. completion date: May 9, 2022
• Est. primary completion date: April 11, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 65 Years to 80 Years

Eligibility

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.

Related Conditions & MeSH terms

• Aging

Intervention

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

Locations

Country	Name	City	State
Canada	Ivor Wynne Centre	Hamilton	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
McMaster University

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in physical activity	7 day steps and activity-related energy expenditure	Baseline, post intervention, 8-week follow-up
Secondary	Change in life-space mobility score	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.	Baseline, post intervention, 8-week follow-up
Secondary	Change in nutrition	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.	Baseline, post intervention, 8-week follow-up
Secondary	Change in feelings of loneliness	The 11-item Revised University of California Los Angeles loneliness scale (R-UCLA) will be used to assess participants' feelings of loneliness.	Baseline, post intervention, 8-week follow-up
Secondary	Change in the Geriatric Depression Scale score	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.	Baseline, post intervention, 8-week follow-up
Secondary	Change in the Geriatric Anxiety Inventory score	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).	Baseline, post intervention, 8-week follow-up
Secondary	Program Feasibility	Program feasibility will be evaluated by: 1) program adherence/attendance in the online exercise program for participants in the intervention group; and 2) program satisfaction/acceptability questionnaire at the end of each online exercise class for all participants in the intervention group.	Throughout the participant's intervention period (0-8 weeks)
Secondary	Participants experiences and perceptions	Participants' experiences and perceptions of exercise and our online exercise program. This will be collected through qualitative data: semi-structured one-on-one interviews conducted with each participant who completes the online exercise program.	1-60 days post intervention