The ADAPT-study: Measuring Physical Performance Using Wearable Sensors in Parkinson's Disease and… (NCT05756075) | Clinical Trial Compass
CompletedNot Applicable
The ADAPT-study: Measuring Physical Performance Using Wearable Sensors in Parkinson's Disease and COPD (ADAPT)
Netherlands154 participantsStarted 2021-12-23
Plain-language summary
The aim of this study is to investigate whether a smartwatch can measure the physical capacity of patients with Parkinson's Disease and COPD in the physiotherapy practice and at home.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Participant is able to read and understand Dutch
* Participant is willing, competent, and able to comply with all aspects of the protocol, including follow-up schedule
* Participant is willing and able to complete patient-reported questionnaires via internet
* Participant can walk
* (PD-specific) Hoehn and Yahr 1-2
* (COPD-specific) Participant has COPD irrespective of airway obstruction severity and has a limited exercise capacity as judged by the physiotherapist
Exclusion Criteria:
* Participant is allergic to nickel
* Participant cannot make an arm swing or is in a situation that prevents arm swing completely
* Co-occurence of COPD and PD
* Participant has cognitive impairment that would prevent understanding and performing tasks in the study
* Participant is pregnant or plans to become pregnant during the course of the study
* Participant is participating in another investigational drug or device study
* Participant has a high fall risk or cardiovascular risk profile
* Participant has any disease or condition that prevents understanding or communication of informed consent, study demands, and testing protocols
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.