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A Study Comparing Smartwatches with Sleep Lab Testing in Adults

To assess the performance of commercially available smart watches with overnight polysomnography in adult population - An observational study - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/06/112565
Enrollment
60
Registered
2026-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

Dr Devendra Chopra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Individual willing to participate in the study with informed consent. 2. Age: between 30 to 60 years suspected of having Obstructive Sleep Apnea (OSA) 3. Both male and female. 4. Individuals with dentulous arch. 5. Individuals with no prior OSA Diagnosis or Treatment

Exclusion criteria

Exclusion criteria: 1. Severe nasal blockage. (e.g., sinusitis, nasal polyps, or deviated septum) 2. Serious medical conditions affecting sleep. (e.g., heart failure, COPD, stroke, Parkinson s) 3. Usage of alcohol, sedatives, or drugs on the day of the test which might alter the study. 4. Patient with insomnia and other sleep disorders.

Design outcomes

Primary

MeasureTime frame
To assess the performance and accuracy of commercially available smartwatches in detecting sleep parameters and obstructive sleep apnea compared with overnight polysomnography (PSG) in adults.Timepoint: 2 years—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactDr Devendra Chopra

Saraswati Dental College and Hospital

chopradevendra@saraswaticolleges.com09045207899

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026