Adapting rHIRE and Sleep Monitoring in Parkinson's Disease (NCT07498296)
Adapting High-Intensity Exercise and Sleep Monitoring Technology for Home Use in Parkinson's Disease
๐ฉบ Plain-English Summary (8th-Grade Level)
Exercise is a primary intervention for symptom management in Parkinson's Disease (PD). However, challenges related to transportation, mobility, and socioeconomic factors often hinder consistent participation in exercise programs. To promote increased access and participation, remote exercise programs offer a promising solution. The investigators previously showed that laboratory-based, high-intensity resistance exercise improves sleep efficiency in individuals with PD in a randomized, controlled, clinical trial. The investigators aim to adapt this protocol for remote delivery and to evaluate the usability of a remote sleep-monitoring device in people with Parkinson's Disease (PwP). Guided by the IDEAS framework for digital health intervention design, the investigators will modify the exercise protocol to ensure safety, accessibility, and fidelity in a home setting. Specific aims include: (1) assessing the adaptability of the HIRE protocol for remote implementation through participant acceptability ratings, adherence, exertion levels, and safety outcomes, (2) evaluating the usability of the Waveband sleep monitoring headband and adherence to night wear schedules, and 3) gather qualitative feedback through semi-structured interviews to understand participant perspectives on protocol design, session completion, and safety. By integrating behavioral theory, participant engagement, and real-world constraints, this research will inform scalable, home-based interventions that are both effective and responsive to the lived experiences of PwP. The findings will lay the groundwork for future clinical trials and broader dissemination of remote therapeutic strategies in neurodegenerative care.
Who can join: Review the eligibility criteria below.
Location: University of Colorado Anschutz Medical Campus โ Aurora, Colorado
Age range: 18 Years
๐งช Interventions in This Study
- High Intensity Resistance Exercise (BEHAVIORAL)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- University of Colorado Anschutz Medical Campus โ Aurora, Colorado
๐ Contact the Study Coordinator
Phone: (805) 886-1854
Email: lina.kleinschmidt@cuanschutz.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in PARKINSON DISEASE (Disorder)
- Autologous Bone Marrow Aspirate (IV) and Bone Marrow Concentrate (Intranasal) for Parkinson's Disease and Parkinson-Plus Syndromes (SPARC-PD) โ Boulder, Colorado
- Prescriptive Infusion Algorithm (PIA) โ Cleveland, Ohio
- SwallowFIT Study in Parkinson's Disease โ San Antonio, Texas
- Treatment of Cognitive and Sensorimotor Deficits in Parkinson's Disease With High Definition Transcranial Direct Current Stimulation โ Richardson, Texas
- Multicontext Approach for Cognitive Function in Parkinson Disease โ St Louis, Missouri
- Virtual tES Device Treatment for Parkinson's Disease Motor Symptoms โ Cleveland, Ohio
Explore by condition: All PARKINSON DISEASE (Disorder) clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.