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Completed

NCT Number: NCT04408287

Improving Activity Engagement Among Persons With SCI During COVID-19

During the current COVID-19 pandemic many spinal cord injury (SCI) rehabilitation services are limited to emergency management, leaving those living in the community without access to services. Unfortunately, this can lead to negative effects including increase in emotional distress, feelings of isolation, and decreased activity engagement. Due to their limited mobility and greater likelihood of respiratory illness it is imperative to provide alternative forms of activity engagement to reduce their risk for secondary complications. Physical activity has been demonstrate to have numerous benefits for individuals with SCI ranging from enhanced health through prevention of secondary complications to improved subjective well-being. The current study proposes to provide an online physical activity program through web-based videoconferencing to person with SCI to improve overall wellbeing and activity engagement. The program will consist of six weeks of twice-weekly, 45-minute sessions in which an experienced fitness instructor (i.e., wheelchair aerobics) with lived experience and a Kinesiology graduate student will lead online sessions. The sessions will be comprised of a 10-minute warm-up phase, a 25-minute aerobic phase and a 10-minute cool-down phase that will incorporate upper-extremity flexibility exercises and guided meditation. In all cases, remote (i.e., in-home) participant monitoring of physiological signals will be conducted by the instructor to ensure safety of participants. Once the program has been completed, participants will be asked to complete self-report questionnaires related to acceptability, feasibility, and limited effectiveness. Participants will also be asked to complete a brief semi-structured interview examining barriers and facilitators of the program. Participant feedback from the interviews will be used to further develop of the program to meet the needs of the population and develop sustainable approaches for access to care in the community setting through collaborations with community partners (SCI Ontario, National SCI Alliance, Ontario Neurotrauma Foundation). Ultimately, the proposed project aims to improve overall wellbeing and access to health care service for those with SCI during the COVID-19 quarantine.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

St. Josephs Parkwood Institute

London, Ontario, N6C 5J1, Canada

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult 18 years or older; living with a spinal cord injury; living in the community in Ontario; access to a computer and internet

Exclusion criteria

  • Not cleared by a physician to participate

Treatment and study plan

WebEx Physical Activity Program

Other

The program will be delivered twice-weekly through 45-minute sessions over 6 weeks. An experienced fitness instructor with lived experience and a graduate student from the Department of Health and Rehabilitation Sciences, will lead a class of 4-6 participants. The sessions will be comprised of a 10-minute warm-up phase, a 25-minute aerobic phase and a 10-minute cool-down phase that will incorporate upper-extremity flexibility exercises and mindfulness meditation. Over the duration the instructor will be sensitive to varying levels of function and fitness and will structure the classes to enable a slow progression of intensity. Individual semi-structured interviews will be completed over the WebEx platform to garner feedback and improve study programming for future implementation of a health care service at Parkwood Institute Outpatient Clinic.

Primary outcomes

  1. Treatment Satisfaction

    Time frame: 6 weeks

    Treatment Satisfaction Questionnaire

Secondary outcomes

  1. Ability to Participate in Social Roles and Activities

    Time frame: Baseline, 6 weeks, and at 3 month follow-up

    Spinal Cord Injury - Quality of Life Short Form

  2. Fatigue

    Time frame: Baseline, 6 weeks, and at 3 month follow-up

    Spinal Cord Injury - Quality of Life Short Form

  3. Satisfaction with Social Roles and Activities

    Time frame: Baseline, 6 weeks, and at 3 month follow-up

    Spinal Cord Injury - Quality of Life Short Form

  4. Positive Affect and Well-Being

    Time frame: Baseline, 6 weeks, and at 3 month follow-up

    Spinal Cord Injury - Quality of Life Short Form

  5. Pain Interference

    Time frame: Baseline, 6 weeks, and at 3 month follow-up

    Spinal Cord Injury - Quality of Life Short Form

  6. Resilience

    Time frame: Baseline, 6 weeks, and at 3 month follow-up

    Spinal Cord Injury - Quality of Life Short Form

  7. Self-Esteem

    Time frame: Baseline, 6 weeks, and at 3 month follow-up

    Spinal Cord Injury - Quality of Life Short Form

Other outcomes

  1. Fear of COVID-19 Scale

    Time frame: Baseline, 6 weeks, and at 3 month follow-up

    Fear of COVID-19 Scale

Sponsors and collaborators

Lead sponsor

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Other

Registry information

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
May 29, 2020
Registry last updated
Mar 15, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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