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An Exploratory Study: Early Mobilization Practices in ICUs at AIIMS, New Delhi

An exploratory study to assess the existing practices and barriers to early mobilization among patients and healthcare providers with a view to develop early mobilization protocol in selected ICUs of AIIMS, NEW DELHI - E-MOTION ICU

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/05/111048
Enrollment
100
Registered
2026-05-26
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Lipika Roy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion Criteria for Patients Adults aged 18 years or older admitted to the ICU. Patients who have been mechanically ventilated during their ICU stay. Patients who have undergone or are eligible for early mobilization interventions. Patients who are medically stable enough to participate in interviews or mobility activities, as judged by attending clinicians. Patients who have been successfully extubated or weaned from mechanical ventilation for qualitative interviews about their experience. Ability to provide informed consent or have a legal representative provide consent on their behalf. Inclusion Criteria for Healthcare Providers: Healthcare professionals currently working in ICU settings, including physicians, nurses, physiotherapists, Minimum of 1 year of experience working in adult intensive care units. Involved directly or indirectly with patient care and mobilization protocols. Willingness to participate and provide informed consent.

Exclusion criteria

Exclusion criteria: For Patients Patients who are too medically unstable to safely participate in early mobilization. Patients unable to provide informed consent and without a legal representative to consent on their behalf. Patients who refuse participation in the study. For Healthcare Providers: Healthcare providers with less than 1 year of ICU experience. Those unwilling or unable to provide informed consent. Providers not involved in direct or indirect patient mobilization or critical care.

Design outcomes

Primary

MeasureTime frame
To assess the existing practices to early mobilization in the selected ICU of AIIMS, New DelhiTimepoint: Single point in time—

Secondary

MeasureTime frame
To identify major facilitators & barriers to early mobilization in the selected ICU. To evaluate associations between patient outcomes & early mobilization efforts Timepoint: Single point in time—

Countries

India

Contacts

Public ContactMs Sibi Riju

College of Nursing, AIIMS New Delhi

sibiriju@gmail.com9958879808

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026