OURA Ring Wearable Testing in MDS Patients: a Feasibility and Discovery Pilot Study OURA MDS

What's the purpose of this trial?

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.

This is an upcoming trial that has not yet started accepting patients.

What will happen during the trial?

You may be able to join this trial if you:

The following criteria is a partial list of reasons why patients may be eligible to participate in this clinical trial. Further evaluation with a medical professional is required.

Inclusion Criteria:

* 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)
* Able to provide informed consent
* Diagnosed with Myelodysplastic Syndrome using WHO 2022 criteria (12)
* Ability to wear the OURA ring and operate the associated smart-phone app, and willing to adhere to the study regimen
* Willing to operate and charge a smart phone loaded with the OURA ring app

Exclusion Criteria:

* Performance status ECOG \> 3.
* Cognitive or physical impairment preventing the usage or utilization of the OURA ring and smart phone.

Additional Trial Information

Observational Trial

Enrollment: 60 patients (estimated)

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