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The Seniors COvid-19 Pandemic and Exercise Study

The Seniors COvid-19 Pandemic and Exercise Study: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04412343
Acronym
SCOPE
Enrollment
241
Registered
2020-06-02
Start date
2020-05-23
Completion date
2020-10-05
Last updated
2020-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Loneliness, Physical Activity, Physical Health, Quality of Life, Social Identification, Well-Being (Psychological Flourishing)

Brief summary

The purpose of this study is to evaluate different types of exercise programs (virtual group-based exercise program; personal exercise program; wait-list control) across 12-weeks on the physical and mental health of older adults during the current Covid-19 pandemic.

Interventions

BEHAVIORALVirtual Group Intervention

Participants will receive weekly exercise courses delivered virtually to a group of older adults. This intervention will last for 12 weeks. Participants in addition to participating in exercise will have designated time after each exercise class to socially connect. Participants in this condition will also receive a t-shirt.

BEHAVIORALPersonal Exercise Intervention

Participants will receive weekly exercise courses delivered virtually. These classes will be pre-recorded so the individual can complete sessions at any time that is convenient for them.

Sponsors

University of Victoria
CollaboratorOTHER
University of British Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

No experimenter or investigator expectancy effects as all assessment occurs online (i.e., online questionnaire). Personnel who analyze the data collected from the study are not aware of the treatment applied to any given group.

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 65+ years old * be able to speak and read English * one participant in the study per household (Spouses, significant others, or family members can take part in the exercise programs with the study participant; however, they will not be able to provide data and won't be remunerated for participating) * not experience any contraindication which might prevent that person from participating in moderate-intensity physical activity. * participants must be able to access the internet at home via a personal smartphone, tablet (e.g., ipad), or computer (device used must have camera capabilities) * low active individuals (i.e., less than 150 minutes of moderate-to-vigorous physical activity per week) * currently living in Canada

Exclusion criteria

* age of less than 65 years * unable to read and speak in English * inability to participate in moderate-to-vigorous physical activity (including a lack of ability to receive doctor's clearance for participating in physical activity) * lack of internet access which does not allow them to access online materials * device used to access the internet does not have a camera/video capabilities * active individuals (e.g., participate in greater than 150 minutes of moderate-to-vigorous physical activity each week) * living outside Canada * not the first person from a household to enroll in the study

Design outcomes

Primary

MeasureTime frameDescription
Well-Being (Psychological Flourishing)Baseline (Week 0), Week 2, Week 4, Week 6, Week 8, Week 10, Follow-up (Week 12)Well-being will be self reported using an 8-item measure from Diener et al., 2010

Secondary

MeasureTime frameDescription
StressBaseline (Week 0), Week 2, Week 4, Week 6, Week 8, Week 10, Follow-up (Week 12)1 Item Statistics Canada Stress Question from the Canadian Community Health Survey (2012)
DepressionBaseline (Week 0), Week 2, Week 4, Week 6, Week 8, Week 10, Follow-up (Week 12)10 Item Center for Epidemiologic Studies Depression Scale (CES-D) via Andresen et al., 1994
ResilienceBaseline (Week 0), Week 2, Week 4, Week 6, Week 8, Week 10, Follow-up (Week 12)6 item Brief Resilience Scale by Smith et al., 2008
Social IdentificationBaseline (Week 0), Week 2, Week 4, Week 6, Week 8, Week 10, Follow-up (Week 12)items adapted from the 4-item scale by Doosje et al., 1995
Social and Emotional LonlinessBaseline (Week 0), Week 2, Week 4, Week 6, Week 8, Week 10, Follow-up (Week 12)11-item scale by De Jong Gierveld et al., 2006
Chronic Illness (Physical Health)Baseline (Week 0)question by Charles et al., 2006 adapted from Larsen et al., 1991
Life SatisfactionBaseline (Week 0), Week 2, Week 4, Week 6, Week 8, Week 10, Follow-up (Week 12)1-item question by Fleeson, 2004
Leisure-time physical activityBaseline (Week 0), Week 2, Week 4, Week 6, Week 8, Week 10, Follow-up (Week 12)modified version of the Leisure Score Index (LSI; Courneya, Jones, Rhodes, & Blanchard, 2004) that has been applied to Godin's Leisure Time Exercise Questionnaire (GLTEQ; Godin & Shepard, 1985).
Alcohol HabitsBaseline (Week 0), Week 2, Week 4, Week 6, Week 8, Week 10, Follow-up (Week 12)3-item measure for alcohol consumption from CDC Behavioral Risk Factor Surveillance System Survey Questionnaire, 1984-2019
Physical AdherenceLooked at each day of the week for 12 weeks to see if a session was attendedObjective measure of attendance in online sessions (interventions conditions only)
Affective AttitudesBaseline (Week 0), Week 2, Week 4, Week 6, Week 8, Week 10, Follow-up (Week 12)3 semantic differential items toward physical activity using scale by Azjen, 2006
DemographicsBaseline only (Week 0)Items addressing sex/gender, age, ethnicity, sexual orientation, chronic conditions, smoking behaviour, height, weight, education level, household income level, employment status, marital status, and living situation (i.e., alone vs. others).
Weekly Somatic Symptoms (Physical Health)Baseline (Week 0), Week 2, Week 4, Week 6, Week 8, Week 10, Follow-up (Week 12)question by Charles et al., 2006 adapted from Marmot et al., 1997

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026