Efficacy and safety of family members participate in the early mobilization of critically ill patients: a randomized controlled trial

The situation and effect of family members participate in the early rehabilitation of critically ill patients

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000028902

Enrollment

Unknown

Registered

2020-01-06

Start date

2020-02-01

Completion date

Unknown

Last updated

2020-06-22

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

Conditions

critically ill patient

Interventions

experimental group:Family members participate in the patient's rehabilitation exercise and usual care

control group:usual care

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Aged >= 18 years; (2) Mechanical ventilation time >= 48h; (3) GCS score >= 11; (4) Patients and their families volunteered to participate in the study.

Exclusion criteria

Exclusion criteria: (1) hemodynamic instability; (2) intracranial pressure >= 20mmHg; (3) active bleeding; (4) unstable fracture, disability and limb movement dysfunction; (5) pregnancy; (6) rupture of aortic aneurysm; (7) the patient or family member has participated in a similar rehabilitation activities.

Design outcomes

Primary

Measure	Time frame
delirium;ICU- acquired weaakness;ICU acquired infection;mortality;	—

Countries

China

Contacts

Public ContactYuchen Wu

The First Hospital of Lanzhou University

yuchen0723@126.com+86 18719782437

Outcome results

None listed

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