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Physical Activity Before Obesity Surgery (PABOS)

G

Göteborg University

Status

Completed

Conditions

Physical Activity
Obesity

Treatments

Other: Increased physical activity
Other: Standard care

Study type

Interventional

Funder types

Other

Identifiers

NCT03641027
FoU i VGR: 202291

Details and patient eligibility

About

There are limited knowledge about the impact of increased pre-operative physical training on postoperative physical activity levels as well as on recovery and complication rates after bariatric surgery.

The primary aim of this study is to investigate whether an intervention including individual coaching to improve level of physical activity before and after gastric bypass surgery leads to a changed of level physical activity post-operatively at eight weeks, one and two years.

Secondary aims of the study are to investigate whether increased physical activity has effects on complication rates, re-admissions and re-operations, post-operative weight-loss, gastrointestinal pain, recovery measured as hospital stay, sick-leave and QoL, resumption of normal physical activity.

METHODS 300 patients will be recruited and randomized to an intervention group or control group. The patients in the intervention group will receive individual coaching by a physical therapist to:

  • increase physical activity 30 minutes/day (At least 150 min/week)
  • decrease time spent sitting/lying The patients in the control group will receive standard care.

Before surgery, 6 weeks, and one year after surgery patient will fill in a questionnaire including level of physical activity, sick leave, quality of life and gastrointestinal pain. In addition blood test will be taken and complication rates recorded.

Enrollment

150 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criterion:

  • Patients at including hospitals scheduled for gastric bypass surgery

Exclusion Criteria:

  • Inability to understand given information.
  • Inability to perform the intervention

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

150 participants in 2 patient groups

Increased physical activity
Experimental group
Description:
Increased physical activity daily before surgery. Standard care during hospital stay and continued training after discharge.
Treatment:
Other: Increased physical activity
Standard care
Other group
Description:
Standard care
Treatment:
Other: Standard care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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