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Protein Supplementation Impact On Body Muscle Mass And Fat Mass In Qataris Post Bariatric Surgery, Randomized Controlled Trials (Rct)

Primary Purpose

Obesity

Status
Unknown status
Phase
Not Applicable
Locations
Qatar
Study Type
Interventional
Intervention
(Cubitan Protein, Nutricia, Netherlands).
(preOp, Nutricia, Netherlands).
Sponsored by
Hamad Medical Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Obesity focused on measuring bariatric, obesity, protein supplements

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Study participants must have the following criteria in order to participate in the trial:

  1. Qatari males or females.
  2. Aged between 18 and 60 year
  3. Based at the bariatric surgery list of HMC with their follow up scheduled be at HMC.

Exclusion Criteria:

Patients will be excluded from participating in the trial if they have the following criteria:

  1. Any Renal or liver disease because that will affect protein or albumin level in body.
  2. Past history of bariatric surgery
  3. Patients will be further excluded after starting the trial if they fall into the following categories:

    • Subjects who did not take at least 80% of their intervention product amount per day, or
    • Subjects who did not comply with the treatment (or placebo) for more than 3 days per week.

Also, patients who refuse to participate & patients with baseline tests showing they are in need for protein supplements will be excluded from the study and given the needed protein supplements per the standard care.

Sites / Locations

  • sahar Dahawi AlshamariRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Intervention group

Control group

Arm Description

Patients will receive nutritional counseling by a bariatric dietitian in a routine round, aiming that they will know the post-surgery diet stages and to not develop any nutritional deficiencies.Before discharge from the hospital, patients will receive supplement and will be advised by the dietitian regarding its use (one can per day, over 3-5 intervals). Supplement contains (per 200 ml can) 20 g of protein, 250Kacl plus different micronutrient and macronutrient (Cubitan Protein, Nutricia, Netherlands).

Patients will receive nutritional counseling by a bariatric dietitian in a routine round, aiming that they will know the post-surgery diet stages and to not develop any nutritional deficiencies. Before discharge from the hospital, patients will receive supplement and will be advised by the dietitian regarding its use (one can per day over 3-5 intervals).Following hospital discharge, Control patients will receive supplement contains per can (200 ml), 0g protein, fat free, 100 kcal and enriched with electrolytes (preOp, Nutricia, Netherlands).

Outcomes

Primary Outcome Measures

Measurement of changes in Body Weight
Measurement of changes in Body Weight
Measurement of changes in Muscle mass.
Measurement of changes in Muscle mass.
Measurement of changes in Fat mass.
Measurement of changes in Muscle mass.

Secondary Outcome Measures

To assess the measurement on Protein
To assess the measurement on Protein
To assess the measurement on Vitamin B12
To assess the measurement on Vitamin B12
To assess the measurement on Magnesium
To assess the measurement on Magnesium
To assess the Zinc level measurement
To assess the Zinc level measurement

Full Information

First Posted
April 18, 2017
Last Updated
May 9, 2017
Sponsor
Hamad Medical Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT03147456
Brief Title
Protein Supplementation Impact On Body Muscle Mass And Fat Mass In Qataris Post Bariatric Surgery, Randomized Controlled Trials (Rct)
Official Title
Protein Supplementation Impact On Body Muscle Mass And Fat Mass In Qataris Post Bariatric Surgery, Randomized Controlled Trials (Rcts)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Unknown status
Study Start Date
March 8, 2017 (Actual)
Primary Completion Date
August 1, 2017 (Anticipated)
Study Completion Date
August 1, 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hamad Medical Corporation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
One of the most common post-operative deficiencies or complications of bariatric surgery is protein malnutrition. It may lead to many predicaments such as malnutrition, vitamin, micro- and macronutrient deficiencies that can lead to deleterious consequences. A protein-rich diet make a person feel satiety and thereby the consumption will be low in overall energy intake. The objectives of our study are. The aim of this study is to assess the effect of protein supplementation on changes in health parameters such as fat mass, muscle mass, weigh change, protein (total and albumin), Vit B12, Zinc and Magnesium, in Qatari patients post bariatric surgery. Our participants are Qatari aged 18-45 years males and females recruited from the bariatric surgery centers of 2 major HMC hospitals (HGH hospital) and will be randomized to receive either the protein supplement (treatment group) or a dietary advice (control group). All participants will be equally followed and monitored for 3 months and data on the above parameters will be collected, together with other population characteristics, at Baseline, 1 month and 3 month. Data will then be analyzed using the most up-to-date SPSS statistical package to assess the effect of protein supplementation on the parameters of interest. Statistical measures will be carefully chosen to properly assess the difference in the treatment (protein supplementation) effect compared with the control (Dietary advice). Investigators hypothesize that Patients receiving protein supplement (intervention group) Compared with patient not on protein supplement (placebo group) will maintain weight loss and other essential health parameters.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
bariatric, obesity, protein supplements

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Masking Description
Investigators and researchers in this study will be blinded to the intervention, i.e. they will not be aware of who is on protein supplement and who is on placebo. Patients will also be blinded to the intervention, i.e. they will not know whether they are taking protein or zero protein supplement. For the blinding there will be a dietician who will assign the treatment and the control to patients as per the above randomization results. This dietician will also be responsible for filling the intervention & control ready-to-feed shakes into identical bottles labeled either A or B, the dietician will not have any other responsibility such as data entry or follow up of participants as this will be done by the PI and research team, he will only be responsible for the blinding process.
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Patients will receive nutritional counseling by a bariatric dietitian in a routine round, aiming that they will know the post-surgery diet stages and to not develop any nutritional deficiencies.Before discharge from the hospital, patients will receive supplement and will be advised by the dietitian regarding its use (one can per day, over 3-5 intervals). Supplement contains (per 200 ml can) 20 g of protein, 250Kacl plus different micronutrient and macronutrient (Cubitan Protein, Nutricia, Netherlands).
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
Patients will receive nutritional counseling by a bariatric dietitian in a routine round, aiming that they will know the post-surgery diet stages and to not develop any nutritional deficiencies. Before discharge from the hospital, patients will receive supplement and will be advised by the dietitian regarding its use (one can per day over 3-5 intervals).Following hospital discharge, Control patients will receive supplement contains per can (200 ml), 0g protein, fat free, 100 kcal and enriched with electrolytes (preOp, Nutricia, Netherlands).
Intervention Type
Dietary Supplement
Intervention Name(s)
(Cubitan Protein, Nutricia, Netherlands).
Intervention Description
Supplement contains (per 200 ml can) 20 g of protein, 250Kacl plus different micronutrient and macronutrient.
Intervention Type
Dietary Supplement
Intervention Name(s)
(preOp, Nutricia, Netherlands).
Intervention Description
contains per can (200 ml), 0g protein, fat free, 100 kcal and enriched with electrolytes
Primary Outcome Measure Information:
Title
Measurement of changes in Body Weight
Description
Measurement of changes in Body Weight
Time Frame
3 months
Title
Measurement of changes in Muscle mass.
Description
Measurement of changes in Muscle mass.
Time Frame
3 months
Title
Measurement of changes in Fat mass.
Description
Measurement of changes in Muscle mass.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
To assess the measurement on Protein
Description
To assess the measurement on Protein
Time Frame
3 months
Title
To assess the measurement on Vitamin B12
Description
To assess the measurement on Vitamin B12
Time Frame
3 months
Title
To assess the measurement on Magnesium
Description
To assess the measurement on Magnesium
Time Frame
3 months
Title
To assess the Zinc level measurement
Description
To assess the Zinc level measurement
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Study participants must have the following criteria in order to participate in the trial: Qatari males or females. Aged between 18 and 60 year Based at the bariatric surgery list of HMC with their follow up scheduled be at HMC. Exclusion Criteria: Patients will be excluded from participating in the trial if they have the following criteria: Any Renal or liver disease because that will affect protein or albumin level in body. Past history of bariatric surgery Patients will be further excluded after starting the trial if they fall into the following categories: Subjects who did not take at least 80% of their intervention product amount per day, or Subjects who did not comply with the treatment (or placebo) for more than 3 days per week. Also, patients who refuse to participate & patients with baseline tests showing they are in need for protein supplements will be excluded from the study and given the needed protein supplements per the standard care.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sahar Dahawi Alshamari
Phone
66655122
Email
Salshamari1@hamad.qa
First Name & Middle Initial & Last Name or Official Title & Degree
Fahad Hanna
Phone
70561906
Facility Information:
Facility Name
sahar Dahawi Alshamari
City
Doha
ZIP/Postal Code
00974
Country
Qatar
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
fahad hanna
Phone
70561906

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29423219
Citation
Al-Shamari SD, ElSherif MA, Hamid W, Hanna F. The effect of protein supplementation on body muscle mass and fat mass in post-bariatric surgery: a randomized controlled trial (RCT) study protocol. Arch Public Health. 2018 Jan 22;76:7. doi: 10.1186/s13690-017-0252-2. eCollection 2018.
Results Reference
derived

Learn more about this trial

Protein Supplementation Impact On Body Muscle Mass And Fat Mass In Qataris Post Bariatric Surgery, Randomized Controlled Trials (Rct)

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