← Back to Clinical Trials
Recruiting NCT06222151

NCT06222151 Recovering From Bariatric Surgery: the Effects of Early Initiated and Supervised Mobilization

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06222151
Status Recruiting
Phase
Sponsor Esbjerg Hospital - University Hospital of Southern Denmark
Condition Postoperative Pain, Acute
Study Type INTERVENTIONAL
Enrollment 112 participants
Start Date 2024-04-22
Primary Completion 2027-06-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 70 Years
Study Type INTERVENTIONAL
Interventions
Intervention 1: Mobilization during hospitalizationIntervention 2: Mobilization the first 4 postoperative weeksControl group

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 112 participants in total. It began in 2024-04-22 with a primary completion date of 2027-06-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The aim is to investigate the effect of early initiated and supervised mobilization continued after discharge as management of postoperative pain and recovery following obesity surgery, including patient experiences, pain coping, physical functionality and quality of life.

Eligibility 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

Contact & Investigator

Central Contact

Nanna Marie Christiansen

✉ nanna.marie.christiansen2@rsyd.dk

📞 +45 20670937

Frequently Asked Questions

Who can join the NCT06222151 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 70 Years, studying Postoperative Pain, Acute. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06222151 currently recruiting?

Yes, NCT06222151 is actively recruiting participants. Contact the research team at nanna.marie.christiansen2@rsyd.dk for enrollment information.

Where is the NCT06222151 trial being conducted?

This trial is being conducted at Esbjerg, Denmark.

Who is sponsoring the NCT06222151 clinical trial?

NCT06222151 is sponsored by Esbjerg Hospital - University Hospital of Southern Denmark. The trial plans to enroll 112 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology