Effects of early mobilization on recovery after obesity surgery
Recovering From Bariatric Surgery: the Effects of Early Initiated and Supervised Mobilization
This study tests if getting up and moving around soon after obesity surgery helps patients recover faster and feel less pain.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 112 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Sponsor | Esbjerg Hospital - University Hospital of Southern Denmark Academic / other |
| Locations | 1 site (Esbjerg, Region Syddanmark) |
| Trial ID | NCT06222151 on ClinicalTrials.gov |
What this trial studies
This study investigates how early and supervised mobilization affects postoperative pain management and recovery in patients who have undergone bariatric surgery. It includes a randomized controlled trial to assess the impact of mobilization during hospitalization and the first four weeks post-surgery. Additionally, it explores patient experiences with mobilization and its influence on pain coping, physical functionality, and overall quality of life. Participants will be randomized into intervention and control groups, and qualitative interviews will be conducted to gather insights on their experiences.
Who should consider this trial
Good fit: Ideal candidates are patients who are undergoing bariatric surgery and can read and understand Danish.
Not a fit: Patients with preoperative dependence on walking aids or significant acute complications may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve pain management and recovery outcomes for patients after bariatric surgery.
How similar studies have performed: Other studies have shown positive outcomes with early mobilization in postoperative recovery, suggesting this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * The ability to read and understand the Danish language Exclusion Criteria: * Preoperative dependence of walking aids * Vision impairment * Previous syncopes or epilepsy * Admission to the intensive care unit after surgery * Acute complications during hospital admission * Patients are excluded at baseline if they have an oxygen saturation below 90% or a systolic blood pressure above 180 mmHg
Where this trial is running
Esbjerg, Region Syddanmark
- Esbjerg Hospital, University Hospital of Southern Denmark — Esbjerg, Region Syddanmark, Denmark (Recruiting)
Study contacts
- Study coordinator: Nanna Marie Christiansen
- Email: nanna.marie.christiansen2@rsyd.dk
- Phone: +45 20670937
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.