Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07498296

Adapting High-Intensity Exercise and Sleep Monitoring Technology for Home Use in Parkinson's Disease

Led by University of Colorado, Denver · Updated on 2026-05-15

16

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating a home-based, high-intensity resistance exercise program combined with remote sleep monitoring for people living with Parkinson's Disease (PD). This study aims to adapt a previously tested laboratory exercise protocol for safe and effective use at home, addressing barriers like transportation and mobility. The research also explores how participants use a sleep-monitoring headband to better understand sleep quality and supports future remote therapeutic strategies in neurodegenerative care. The intervention involves performing five upper and lower body resistance exercises, each with 10 repetitions for 3 sets, including additional bodyweight exercises between sets. The program is delivered remotely, allowing participants to exercise at home with internet access and a video-capable device. The study also assesses the usability and adherence to a sleep-monitoring headband worn at night. The exercise intervention lasts for three sessions, with participant feedback collected via surveys and interviews shortly after completion. Participants will complete acceptability surveys and semi-structured interviews within one week after finishing the exercise program to share their experiences and safety outcomes. The study monitors adherence to the exercise and sleep device use, participant exertion levels, and safety measures. The total study duration is based on completing the three exercise sessions and follow-up assessments, with the goal of developing accessible, home-based exercise and monitoring approaches for people with Parkinson's Disease.

CONDITIONS

Brief Title

Adapting rHIRE and Sleep Monitoring in Parkinson's Disease

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Currently residing in Colorado, USA
  • Diagnosed with Parkinson's Disease per Movement Disorders Society Diagnostic Criteria
  • Requires less than minimal assistance at home
  • Has internet access
  • Has a video-capable device
Not Eligible

You will not qualify if you...

  • Uncontrolled cardiovascular or pulmonary disease
  • Musculoskeletal injuries
  • Participating in Parkinson's Disease community exercise programs more than 3 days a week
  • Contraindication to physical activity per Physical Activity Readiness Questionnaire (PAR-Q)
  • High fall risk defined by taking more than 20 seconds to complete the 5 times sit to stand test or frequent falls (one or more per month) in the past year
  • Virtual Montreal Cognitive Assessment (MoCA) score less than 18 at eligibility visit

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

Duration - 3 weeks

Participants engage in a high intensity resistance exercise program involving 5 upper and lower extremity resistance exercises with additional body weight exercises.

1 baseline visit and 1 follow-up visit

Trial Site Locations

Total: 1 location

1

University of Colorado Anschutz Medical Campus

Aurora, Colorado, United States, 80004-4159

Actively Recruiting

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Research Team

L

Lina Kleinschmidt, DPT

A

Aya Miften, BS

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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