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Exercise to Improve Sleep in Parkinson's Disease

Parkinson Disease

This study will investigate the impact of three common exercise modalities, cardiovascular, resistance, and multimodal (i.e., a combination of the previous two) training, on sleep quality and architecture in persons with Parkinson's disease (PD). Furthermore, the project will investigate whether the potential positive exercise-induced changes in sleep are associated with improvements in different quality of life (QoL)-related aspects. Participants will perform either cardiovascular training (CT), resistance training (RT), multimodal training (MT), or will be allocated to a control condition (i.e., waiting list - CON) for 12 weeks. Training will be performed three times/week. The assessments will be conducted at baseline, post-intervention, and follow-up (i.e. 8 weeks after the intervention) by assessors blinded to the participants' group allocation.

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Participation Requirements

  • Sex:

    ALL

  • Eligible Ages:

    40 and up

Participation Criteria

Inclusion Criteria:

* Persons with mild-moderate idiopathic Parkinson's Disease (Modified Hoehn \& Yahr Scale stages 0.5-3.5);
* On a stable dosage of medication during the previous month;
* Having poor sleep quality defined as a score \> 15 in the PDSS-2;

Exclusion Criteria:

* Having atypical parkinsonism, dementia, stroke, or any other neurological condition;
* Presenting severe untreated obstructive sleep apnea (OSA);
* Having a Montreal Cognitive Assessment (MoCA) score \<18
* Having a Beck Depression Inventory score \>31;
* Having absolute contraindications to exercise;
* Having severe osteoporosis;
* Participating in an exercise or drug trial during the period of the study;
* Exceeding the physical activity levels recommended for the general population (≥150 minutes/week of moderate-intensity or ≥75 minutes/week of vigorous-intensity cardiovascular activity) and/or strengthening activities ≥2 days/week.

Study Location

Cummings Centre
Cummings Centre
Montréal, Quebec
Canada

Contact Study Team

Primary Contact

Maria Fragapane

[email protected]
514.734.1797
Human Brain Control of Locomotion Laboratory
Human Brain Control of Locomotion Laboratory
Montréal, Quebec
Canada

Contact Study Team

Backup Contact

Alexandra Potvin-Desrochers, Ph.D.

[email protected]
514-398-4184
Primary Contact

Caroline Paquette, Ph.D.

[email protected]
514-398-4400
Jewish Rehabilitation Hospital
Jewish Rehabilitation Hospital
Laval, Quebec
Canada

Contact Study Team

Backup Contact

Jacopo Cristini, MSc

[email protected]
450-688-9550
Primary Contact

Marc Roig, Ph.D.

[email protected]
450-688-9550
Study Sponsored By
McGill University
Participants Required
More Information
Study ID: NCT05644327