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Effect of Physical Activity on Weight Loss and Cardiovascular Risk Factors After Gastric Bypass

Not Applicable
Completed
Conditions
Morbid Obesity
Inactivity
Interventions
Behavioral: Physical Activity
Registration Number
NCT01690728
Lead Sponsor
Esbjerg Hospital - University Hospital of Southern Denmark
Brief Summary

The aim of this study is to increase our knowledge about the effect of physical activity in patients who have undergone gastric bypass surgery. The study will provide novel information in two areas. The main objective is to study the effect of physical activity on the weight loss and cardiovascular risk factors. This will be accomplished in a randomized clinical trial in patients, who are eligible for gastric bypass (GB). Patients will be randomized to six month of structured physical activity or standard postoperative counseling. The study will include an exhaustive panel of blood tests related to cardiovascular risk and the most extensive evaluation of structural and functional vascular test done in this patient group so far. In addition the study will provide information of the effect of bariatric surgery per se since both pre- and postoperative investigations are conducted. The study will learn us to what degree it is possible to motivate this group of patients to increased physical activity. All together this will enable us to improve the counseling of the patients undergoing GB.

Detailed Description

The study will be conducted as a prospective, randomized, controlled, two-group, intervention study. Patients will be recruited among individuals referred to the tertiary center for bariatric surgery. The patients will be asked to participate in the study when they attend the preoperative education for bariatric surgery. Randomization will be performed in blocks ensuring an equal distribution of type 2 diabetes patients in the two study groups.

Participants will be investigated before gastric bypass surgery, six, 12 and 24 month post-operative. Intervention, consisting of structured physical activity will take place from six to 12 month after operation.

The intervention program will continue for six month. The supervised exercise program will take place at the training center consisting of 40 min. sessions two times pr. week for 26 consecutive weeks.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Age 25 - 60 years
  • Able to understand and cooperate with the interventions in the study
  • Eligible for gastric bypass surgery
Exclusion Criteria
  • Inability to perform physical activity at the intensity and quantity required in the study, such as physical disabled patients including severe osteoarthritis
  • Use of vitamin K antagonists, oral contraceptives, or hormone replacement therapy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Physical ActivityPhysical Activity40 min exercise supervised by physiotherapists two times weekly in six month.
Primary Outcome Measures
NameTimeMethod
Weight lossMeasures 1-2 weeks before gastric bypass, change from baseline 6, 12 and 24 month post-surgery

The participants pre-operative weight are measured before gastric bypass surgery. This measure will take place within 2 weeks before surgery. Weight change from baseline will be measured 6, 12 and 24 months post-surgery.

Secondary Outcome Measures
NameTimeMethod
Blood testsMeasures 1-2 weeks before gastric bypass, 6, 12 and 24 month post-surgery

Exhaustive panel of blood tests related to cardiovascular risk. The participants are measured before gastric bypass surgery. This measure will take place within 2 weeks before surgery. Changes in blood analyses from baseline will be measured 6, 12 and 24 months post-surgery.

Trial Locations

Locations (1)

Center of Bariatric Research, Dep. of Endocrinology, Hospital of South West Denmark

🇩🇰

Esbjerg, Denmark

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