OURA Ring Wearable Testing in MDS Patients: a Feasibility and Discovery Pilot Study
Recruiting now
Conditions studied: MDS, Myelodysplastic Syndromes, Myelodysplastic/Myeloproliferative Neoplasms, RARS-T
In brief
A prospective, single center, single arm phase 2 cohort feasibility study of the OURA ring in adult MDS patients. Patients with MDS will wear the OURA ring and upload biometrics weekly. Quality of life measures will be clinically evaluated and correlated with biometrics. We hypothesize that it will be feasible for MDS patients to wear the OURA ring 70% of the time for 3 months.
Key facts
- Study ID
- NCT06270771
- Run by
- Sunnybrook Health Sciences Centre
- People needed
- 60
- Starts
- 2025-03-20
- Expected to finish
- 2027-02-01
- Last updated by the study team
- 2025-07-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Provision of signed and dated informed consent form
- Stated willingness to comply with all study procedures and availability for the duration of the study
- Male or female, aged 18 or older
- Able to read, write and speak English or French (non-English or French speaking patients may participate if appropriate translation is used)
- Diagnosed with Myelodysplastic Syndrome using WHO 2022 criteria (12) all risk groups
- Ability to wear the OURA ring and operate the associated smart-phone app, and willing to adhere to the study regimen
You may not qualify if…
- Performance status ECOG > 3.
- Cognitive or physical impairment preventing the usage or utilization of the OURA ring and smart phone.
Where it is running
- Sunnybrook Health Sciences Research Centre — Toronto, Ontario, Canada (enrolling)
Full record on ClinicalTrials.gov
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