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The Investigation of the Impact of Early Mobilization on the Outcome in Patients With Aneurysmal Subarachnoid Hemorrhage.

NCT06436508 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2024-05-31

No results posted yet for this study

Summary

The goal of the randomized clinical trial is to examine the effect of early mobilization on primary and secondary outcomes in patients with subarachnoid hemorrhage caused by aneurysm rupture.

Researchers will compare early mobiliziation vs. standrad bed rest care.

Conditions

  • Early Ambulation
  • Standard of Care
  • Subarachnoid Hemorrhage, Aneurysmal

Interventions

BEHAVIORAL

Early mobilization protocol

* Step 1 - Day 1: Bed rest, elevation of the head end to 30° * Step 2 - Day 2: Bed rest, elevation of the head end to 60° * Step 3 - Day 3: Bed rest, elevation of the head end to 80° * Step 4 - Day 4: Sitting on the edge of the bed * Step 5 - Day 5: Sitting in a chair, standing up * Step 6 - Day 6: Walking with or without assistance * Step 7 - Day 7: Walking with or without assistance from today

BEHAVIORAL

Standard care

During standard care, early mobilization does not take place in the intensive care unit; the patient receives only standard supportive care in bed rest.

Sponsors & Collaborators

  • National Institute of Mental, Neurological and Neurosurgery

    collaborator UNKNOWN

  • Borsod-Abaúj-Zemplén County Central Hospital and University Teaching Hospital

    collaborator UNKNOWN

  • University of Pecs

    lead OTHER

Principal Investigators

  • Peter Csecsei, MD. PhD · University of Pecs

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-06-14
Primary Completion
2025-01-31
Completion
2026-03-31

Countries

  • Hungary

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06436508 on ClinicalTrials.gov