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Physical Exercise Prehabilitation Program in MEtabolic SuRgery

Physical Exercise Prehabilitation Program in MEtabolic SuRgery

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06889207
Acronym
PEPPER
Enrollment
58
Registered
2025-03-21
Start date
2022-03-14
Completion date
2026-05-31
Last updated
2025-03-28

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

Conditions

Bariatric Surgery, Exercise, Obesity and Overweight, Physical Fitness, Prehabilitation, Six Minute Walk Test

Brief summary

The goal of this clinical trial is to learn if an exercise program before bariatric surgery works to treat obesity, could improve physical condition and weight loss before bariatric surgery and induce a lifestyle behavior change. The main questions it aims to answer are: * Does a supervised exercise program lead to improved physical condition prior to bariatric surgery? * Does a supervised exercise program prior to bariatric surgery lead to reduced surgery related complications? * Does a supervised exercise program prior to bariatric surgery lead to maintained lifestyle changes after surgery? Participants will: * Receive either no training program or physical exercise training program twice a week, supervised by a physical therapist, for a duration of 8 weeks. * Have their fitness measured at the start and at the end of the 8 weeks, measured with a six minute walking test. * Fill in a survey on their perceived quality of life and exercise habits at the start of the trial, and at 1 year after surgery.

Interventions

BEHAVIORALPhysical exercise prehabilitation

Patients in the intervention group will have two supervised training sessions per week for eight weeks in group sessions supervised by a physiotherapist.

Sponsors

Flevoziekenhuis
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

* Adult patients (≥18 years) * Body-Mass-Index (BMI) 40 kg/m2 or higher, or 35 kg/m2 or higher with the presence of at least one comorbidity (type 2 diabetes, high blood pressure, heart and/or vascular diseases, obstructive sleep apnea (OSA), dyslipidemia, or arthritis). * Primary bariatric patients; without previous bariatric surgery. For inclusion the investigators will follow the National Guidelines on metabolic surgery.

Exclusion criteria

Patients with: * mobility problems (patients who are not able to exercise) * cognitive disabilities * illiteracy (patients who are not able to read and understand the language of the country where the study will be performed)

Design outcomes

Primary

MeasureTime frameDescription
six-minute walk test2 monthsPreoperative physical condition, assessed by using the six-minute walk test (6MWT). The target increase of the 6MWT is 10% in the intervention group.

Countries

Netherlands

Outcome results

None listed

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