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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02631707
Other study ID # Highproteinbariatric
Secondary ID
Status Completed
Phase N/A
First received May 26, 2015
Last updated October 26, 2017
Start date May 2015
Est. completion date August 2016

Study information

Verified date October 2017
Source University of Auckland, New Zealand
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

All patients in CMDHB eligible for bariatric surgery are given a weight loss goal prior to surgery. It is unknown what the most effective diet is to lose weight, while still preserving muscle mass. The diet must also be acceptable and adhered to by patients. The aim of this study is to find out if a diet that is higher in protein and lower in carbohydrate than the standard Ministry of Health guidelines will have a greater effect on weight loss, preservation of lean muscle mass, surgical recovery score, adherence and acceptability.


Description:

This pilot project is a randomised control trial with 24 participants. Diets will consist of 1200 and 1500kcals for females and males, respectively. The control arm is to receive the Ministry of Health guidelines percentage energy from carbohydrate (50-55%), protein (10-15%) and fat (30%). The intervention arm is to be lower in carbohydrate (40%), higher in protein (30%), moderate fat (30%). Participants will be required to continue the diet for at least 8 weeks while waiting for surgery. At baseline and at eight weeks their weight, hip circumference, waist circumference, neck circumference and body composition measurements will be taken. During their prescribed diet they are required to fill out a 3-day diet record. At the end of eight weeks the participants will perform a twenty-four hour urine collect for urea and creatinine. This will help determine adherence. Post-surgery (21-28 days) they will be required to complete a surgical recovery questionnaire and the above measurements will be recorded again. These data will be collected over a period beginning January 2015. It is expected that the intervention arm will have greater weight loss and better preservation of muscle mass leading to a better surgical recovery score. However because the intervention requires a higher intake of protein this may have an effect on adherence and acceptability in these participants. There are no known adverse effects of the intervention diet in the short term.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date August 2016
Est. primary completion date August 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Participants in this study will be patients eligible for bariatric surgery under CMDHB. These participants must have a BMI greater than 35kg/m2 with co-morbidities or a BMI greater than 40kg/m2.

Exclusion Criteria:

- Patients will be excluded from study if they do not attend surgeon or dietitian appointments. To be included in this study patients must be English speaking and weigh under 200kg.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
High protein diet
The intervention diet is higher in protein than the control diet.

Locations

Country Name City State
New Zealand Counties Manukau District Health Board Auckland

Sponsors (2)

Lead Sponsor Collaborator
University of Auckland, New Zealand Counties Manukau Health

Country where clinical trial is conducted

New Zealand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Weight Scales After 8-weeks of diet and 21-28 days post bariatric surgery
Primary Change in Total body muscle mass Biometric scales After 8-weeks of diet and 21-28 days post bariatric surgery
Secondary Surgical recovery score SRS tool Surgical recovery score 21-28 days post surgery
Secondary compliance urinary creatinine 8 weeks
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