Skip to content

A longitudinal study on sleep disorders and their influencing factors in ICU survivors

A longitudinal study on sleep disorders and their influencing factors in ICU survivors

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104131
Enrollment
Unknown
Registered
2025-06-11
Start date
2025-06-12
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Sleep disorder

Interventions

Intervene Group:On the basis of the control group, a sleep follow-up program was carried out to remind patients to wear the sleep wristband every day and check their sleep conditions. For patients wit
Control Group:When patients are admitted to the ICU, they follow the same evidence-based intervention methods as those in the control group. Upon discharge, patients are invited to join a WeChat group

Sponsors

The Affiliated Hospital of Nantong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) Age greater than or equal to 18 years old; (2) ICU stay greater than or equal to 24 h; (3) Conscious and able to communicate normally when transferred out of ICU; (4) Willing to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Mental disorders; (2) advanced diseases with an expected life span of less than 6 months; (3) participation in other intervention studies; (4) ICU survivors who are unable to participate in follow-up surveys due to uncontrollable factors such as disease deterioration; (5) those who voluntarily withdraw during the study; (6) loss of follow-up.

Design outcomes

Primary

MeasureTime frame
Sleep time;PSQI scale scores;

Secondary

MeasureTime frame
Anxiety and depression scale scores;

Countries

China

Contacts

Public ContactJuan Wu

The Affiliated Hospital of Nantong University

texu1910@163.com+86 138 6190 1841

Outcome results

None listed

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