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Structured Physical Activity for Sleep Quality and Daytime Sleepiness in Patients With Parkinson's Disease

Effect of a Structured Physical Activity Program on Sleep Quality and Sleepiness in Parkinson's Disease

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01544465
Enrollment
1
Registered
2012-03-06
Start date
2011-08-31
Completion date
2014-03-31
Last updated
2014-03-21

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

Conditions

Hypersomnia, Parkinson's Disease, Poor Quality Sleep

Keywords

Parkinson's disease, Sleep Quality, Daytime sleepiness, physical therapy, exercise

Brief summary

The purpose of this study is to examine the ability of a structured physical activity program to improve sleep quality and daytime sleepiness in patients with Parkinson's disease.

Detailed description

Parkinson's disease (PD) is a chronic, progressive, neurodegenerative disease that affects 1% of elderly people. Sleep disturbances affect up to 88% of patients with PD and commonly include sleep fragmentation and excessive daytime sleepiness (EDS); these symptoms can significantly impair quality of life. The cause of sleep fragmentation and EDS is likely multifactorial, including medications, neurodegeneration, primary sleep disorders such as sleep apnea, and decreased physical activity. Pharmacotherapy in this population is limited due to side effects and drug-drug interactions. The goal of this project is to develop non-pharmacologic therapies for impaired sleep quality and EDS in PD. Sleep disturbances and EDS are common among patients with PD and negatively affect their quality of life. There is data to support a role for physical activity in sleep in older adults with and without insomnia. Additionally, increased physical activity in patients with PD has been associated with improvement in PD motor symptoms and quality of life. Therefore, the investigators propose to examine the ability of structured physical activity to improve sleep quality and daytime sleepiness in patients with PD. The overall objective of the proposed project is to develop behavioral approaches to improve sleep quality and daytime function in PD. The investigators propose to examine the effect of a structured physical activity program and sleep hygiene education on nighttime sleep quality and EDS in patients with idiopathic PD. There will be two groups: 1) a structured physical activity program with sleep hygiene education (SPA group), and 2) a control group receiving only sleep hygiene education (SH group) who will be offered the delayed physical activity program. The investigators hypothesize that the structured physical activity program will improve subjective and objective sleep quality and daytime sleepiness compared to sleep hygiene education alone.

Interventions

Rehabilitation evaluation and 8 weeks of physical therapy

BEHAVIORALSleep hygiene education

Educational materials on insomnia published by the American Academy of Sleep medicine

Sponsors

Shirley Ryan AbilityLab
CollaboratorOTHER
Northwestern University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Established clinical diagnosis of Hoehn and Yahr stage I to III idiopathic Parkinson's disease, * Male and female. * Age of onset of PD \>= 50 years; * Impaired sleep quality determined by Parkinson's disease sleep scale (PDSS-2) total score ≥ 12; * EDS as determined by Epworth Sleepiness Scale (ESS) \> 10; * Sedentary (\< 30 minutes/day or \< 2 times/week of exercise) based on physical activity history; * Stable on medications for PD for at least 2 months; * After clinical evaluation, was provided with a referral by their Movement Disorders Neurologist for an evaluation at the Movement Disorders Rehabilitation Evaluation Clinic at the Rehabilitation Institute of Chicago.

Exclusion criteria

* Cognitive impairment as determined by Montreal Cognitive Assessment (MoCA) total score \< 25; * High likelihood of sleep disordered breathing as determined by the Berlin Questionnaire (BQ); * Restless legs syndrome (RLS) based on the International RLS Study Group diagnostic criteria; * Current use of any sedative/hypnotics or stimulants, tricyclic antidepressants, and trazodone; * Use of selective serotonin reuptake inhibitors (SSRIs) and bupropion will be allowed only if the patient has been on a stable dose for at least three months; * Unstable medical or psychiatric condition; * History of falls in the last 2 months; * Participants with parasomnias such as Rapid Eye Movement Behavior Disorder will not be excluded as up to 50% of patients with PD have parasomnias and exclusion of these patients would result in difficulty with recruitment and the results would be less generalizable; * Current depression based on BDI-II total score \> 19; * Current occupation involves shift work; * At visit #2, Apnea-hypopnea index \>15 on baseline PSG; * At visit #2, Periodic limb movements in sleep index \>15 on baseline PSG; * At physiatry evaluation at RIC, inpatient rehabilitation is recommended.

Design outcomes

Primary

MeasureTime frame
Change in polysomnographically-derived wake after sleep onsetBaseline and 10 weeks
Change in mean sleep latency test-derived mean sleep latencyBaseline and 10 weeks

Secondary

MeasureTime frameDescription
Change in Pittsburgh Sleep Quality IndexBaseline and 10 weeksThe Pittsburgh Sleep Quality Index is a survey-derived measure of sleep quality.
Change in Epworth Sleepiness ScaleBaseline and 10 weeksThe Epworth Sleepiness Scale is a survey-derived measure of sleepiness

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026