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Timing of Mobilization on Delirium in Patients After Cardiac Surgery

The Effect of Timing of Mobilization on Delirium in Patients After Cardiac Surgery: a Pilot Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06069349
Enrollment
60
Registered
2023-10-05
Start date
2023-09-15
Completion date
2024-12-31
Last updated
2023-10-10

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

Conditions

Patients After Cardiac Surgery

Brief summary

Early mobilization is recommended because it is effective in improving symptoms for patients after cardiac surgery. However, the optimal timing of mobilization for postoperative patients is not unclear. How early is early? As early mobilization in the ICU is safe and may reduce healthcare costs, the goal was to assess the effect of early mobilization in the ICU on the incidence and duration of delirium.

Detailed description

The prevalence of cardiac diseases is high, as the standard treatment for many heart diseases, a bunch of strategies are performed to improve the outcome of cardiac surgery. Early mobilization is recommended because it is effective in improving symptoms for patients after cardiac surgery. However, the optimal timing of mobilization for postoperative patients is not unclear. How early is early? As early mobilization in the ICU is safe and may reduce healthcare costs, the goal was to assess the effect of early mobilization in the ICU on the incidence and duration of delirium.

Interventions

Early Rehabilitation for patients after cardiac surgery

OTHERusual treatment

Patients are not allowed to exercise Early Rehabilitation

Sponsors

Jingyuan,Xu
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 1\. \> 18-year-old postoperative cardiac patient admitted to ICU, the time \< 24h * 2\. Patients agree to participate in clinical research and sign informed consent before the start of the study

Exclusion criteria

Patients who meet any of the following criteria are not eligible for inclusion in this study: * 1\. Pregnant and lactating women * 2\. There are contraindications to getting out of bed: * 2.1 Low cardiac output syndrome * (1) Application of IABP or PCPS (percutaneous cardiopulmonary support) * (2) High doses of vasoactive drugs (norepinephrine\> 0.5ug/kg.min) * (3) SBP\<=80mmHg * (4) Acrocyanosis, wet and cold * (5) Metabolic acidosis * (6) Urine output less than 0.5ml/kg.h for more than 2 hours * 2.2 Heart rate greater than or equal to 120 beats per minute at rest * 2.3 Orthostatic hypotension (systolic blood pressure less than 80 mmHg after postural change) * 2.4 Presence of arrhythmias leading to a drop in blood pressure (e.g., decreased blood pressure due to new-onset atrial fibrillation) * 2.5 Difficulty breathing at rest or respiratory rate greater than 30 breaths per minute * 2.6 Postoperative bleeding (200ml in 2-3 hours)

Design outcomes

Primary

MeasureTime frameDescription
duration of delirum7 daysThe duration of delirum in hours

Secondary

MeasureTime frameDescription
hospital length of stayhospital length of stay, approximately 10 dayshospital length of stay, approximately 10 days

Countries

China

Contacts

Primary ContactJingyuan Xu, M.D.
13851417209@163.com008613851417209

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026