An observational study using wearable device monitoring sleeping state in postoperative patients in ICU

Prospective observational study evaluating effectiveness of using wearable device monitoring sleeping state and related complications in awake postoperative patients in ICU

Status

Active, not recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200060881

Enrollment

Unknown

Registered

2022-06-13

Start date

2022-06-01

Completion date

Unknown

Last updated

2023-03-26

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

Conditions

Sleep disorders in ICU

Interventions

na:na

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years old 2.post-surgical admission to ICU 3.sober or expected to be successfully resuscitated 4.the expected ICU admission time is not less than 10h 5.Signed informed consent form

Exclusion criteria

Exclusion criteria: 1.the presence and sleep-related underlying diseases: including neurological and sleep disorders. 2.Post-neurosurgical patients with Glasgow Coma Score (GCS) 3.Surgery affecting patient mobility, or mandatory bed rest 4.Unstable respiratory circulation (moderate doses of vasoactive drugs to maintain mean arterial pressure 50%, P/F ratio < 100 mmHg) 5.I or family treatment is not active

Design outcomes

Primary

Measure	Time frame
Wearable sleep monitoring parameters;	—

Secondary

Measure	Time frame
Richards-Campbell Sleep Questionnaire,RCSQ;	—

Countries

China

Contacts

Public ContactLi Zhe

slamy1987@126.com+86 13917246870

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026