OURA Ring Wearable Testing in MDS Patients: a Feasibility and Discovery Pilot Study
NCT06270771 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 60
Last updated 2025-07-08
Summary
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.
Conditions
- MDS
- Myelodysplastic Syndromes
- Myelodysplastic/Myeloproliferative Neoplasms
- RARS-T
Interventions
- DEVICE
-
OURA Ring
The OURA ring (https://ouraring.com) is a light-weight wearable device in the form of a ring that has several microsensors enabling detection of heart rate, blood oxygen level, skin temperature, and movement. The OURA ring and application can synthesize the sensory data to generate physiologic information such as sleep, activity level, resting heart rate, heart rate variability, respiratory rate, and more. The OURA ring is water resistant and has up to 5-7 days of battery life and can be fully charged in 20-80 minutes. It communicates with the OURA app and commonly used Smartphone health apps via Bluetooth connectivity with automatic syncing every week.
Sponsors & Collaborators
-
Sunnybrook Health Sciences Centre
lead OTHER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-03-20
- Primary Completion
- 2026-03-20
- Completion
- 2027-02-01
Countries
- Canada
Study Locations
More Related Trials
-
Integrating Touchscreen-based Geriatric Assessment and Frailty Screening for Adults With Multiple Myeloma
NCT03068637 ·Status: COMPLETED ·Phase: NA
-
The Prognostic Value of CPCs Quantified by Flow Cytometry in Patients With Multiple Myeloma: a Prospective, Multicenter Clinical Trial
NCT06228794 ·Status: RECRUITING
-
Treating Anemia in Myelofibrosis With Repurposed Drugs (Nelfinavir) That Restore Iron Delivery to the Bone Marrow
NCT07281781 ·Status: RECRUITING ·Phase: PHASE1/PHASE2
-
Refine and Assess the Readability of Patient, Carer, and Clinician Treatment Preference in Myelodysplasia Questionnaire
NCT05817331 ·Status: COMPLETED
-
Determine PK Profiles of Ozanimod and Its' Major Metabolites in Healthy Subjects
NCT06528665 ·Status: COMPLETED
-
Curcumin to Improve Inflammation and Symptoms in Patients With Clonal Cytopenia of Undetermined Significance, Low Risk Myelodysplastic Syndrome, and Myeloproliferative Neoplasms
NCT06063486 ·Status: RECRUITING ·Phase: PHASE2
-
CC-4047 in Treating Patients With Myelofibrosis
NCT00669578 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
CEP-701 (Lestaurtinib) in Myelofibrosis
NCT00668421 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
Paricalcitol in Treating Patients With Myelodysplastic Syndrome
NCT00064376 ·Status: COMPLETED ·Phase: PHASE2
-
Treating Cancer-Related Fatigue Through Systematic Light Exposure (Light for Fatigue Study)
NCT03119363 ·Status: COMPLETED ·Phase: NA
-
CellCept/Iron Study: The Iron Ion-Mycophenolate Mofetil Chelation Complex Interaction in Renal Allograft Recipients
NCT00227045 ·Status: COMPLETED
-
Intervention for Symptom Burden During Maintenance Therapy for Multiple Myeloma
NCT01793051 ·Status: COMPLETED ·Phase: PHASE2
-
Investigation of Dysregulated Signaling in MPD Via Multiparameter Phospho-specific Flow Cytometry
NCT01144780 ·Status: TERMINATED
-
The Efficacy of Coenzyme Q10 And Curcumin in Patients With Myelodysplastic Syndromes
NCT00247026 ·Status: WITHDRAWN ·Phase: PHASE1/PHASE2
-
Evaluating the Impact of a 12-month Multi-Modal Lifestyle Management Intervention on Disease Relevant Biomarkers
NCT06987708 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
CEP-701 for PH-negative Myelofibrosis
NCT00494585 ·Status: COMPLETED ·Phase: PHASE2
-
Lurbinectedin in Patients With Advanced Gastrointestinal Malignancies With DNA Repair Mutations
NCT05229588 ·Status: COMPLETED ·Phase: PHASE2
-
Study of Disulfiram and Copper Gluconate in Patients With Treatment-Refractory Multiple Myeloma
NCT04521335 ·Status: TERMINATED ·Phase: PHASE1
-
Telehealth Exercise Intervention to Improve Physical Function and Frailty in Multiple Myeloma Survivors
NCT05142371 ·Status: COMPLETED ·Phase: NA
-
Multi-center Study of TBI-1301 (INN: Mipetresgene Autoleucel; Mip-cel) in Patients With NY-ESO-1 Positive Synovial Sarcoma
NCT07174427 ·Status: RECRUITING ·Phase: PHASE3
-
A Study of [14C]-LY4065967 in Healthy Participants
NCT07039045 ·Status: COMPLETED ·Phase: PHASE1
-
A PK Study to Assess the Drug-drug Interaction of a Strong CYP2C8 Inhibitor on Adagrasib
NCT05868356 ·Status: COMPLETED ·Phase: PHASE1
-
Phase II High-Dose Cyclophosphamide for Multiple Sclerosis
NCT00296205 ·Status: WITHDRAWN ·Phase: PHASE2
-
Ph II Study of Azacitidine in Myelofibrosis
NCT00569660 ·Status: COMPLETED ·Phase: PHASE2
-
The Ambient Light Multiple Myeloma Study
NCT05737732 ·Status: RECRUITING ·Phase: NA