Testing the Gravitostat in Humans: the Impact of a Weighted Vest in Patients Post Bariatric Surgery on Fat-free Mass Retention and Weight Loss

Sponsor
University College Dublin (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04809129
Collaborator
(none)
40
2
17.8

Study Details

Study Description

Brief Summary

The mechanisms regulating fat mass homeostasis are incompletely understood although recent animal and human trials would suggest that there is a leptin independent regulatory pathway which may play a role in weight control and maintenance. Although evidence would suggest that external loading in patients with obesity may promote body weight loss, this has not been explored in patients following bariatric surgery.

The aim of this study is to investigate the mechanisms regulating weight loss and the potential role of the 'gravitostat' in fat free mass retention in patients following bariatric surgery.

Condition or Disease Intervention/Treatment Phase
  • Device: Weighted vest
N/A

Detailed Description

The aim of the study is to investigate the mechanisms that regulate weight loss, particularly following bariatric surgery. Previous animal studies have suggested that there is an underlying regulatory process controlled by 'the gravitostat' which is an evolutionary adaptation responsible for weight control and maintenance. Studies exploring this concept in rodent models have suggested that artificially increasing the animal's weight with the implantation of weighted capsules results in greater weight loss in mice with obesity but does not affect those of normal weight. We will use weighted vests in patients following surgery to replicate this increased mechanical loading to determine whether a similar process occurs in humans. This will improve our understanding of the underlying processes regulating weight in patients with obesity and following bariatric surgery.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Testing the Gravitostat in Humans: the Impact of a Weighted Vest in Patients Post Bariatric Surgery on Fat-free Mass Retention and Weight Loss
Anticipated Study Start Date :
Apr 8, 2021
Anticipated Primary Completion Date :
Oct 1, 2022
Anticipated Study Completion Date :
Oct 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: External mechanical loading

Following bariatric surgery (RYGB or SG) patients will be asked to wear a weighted vest for a minimum of 8 hours daily and during physical exercise for three months postoperatively. Weight will be incrementally added on a weekly basis to maintain the baseline weight as patients lose weight following surgery up to a maximum of 15%.

Device: Weighted vest
Patients will wear a weighted vest following bariatric surgery with weight increased incrementally to maintain baseline weight. This vest will be worn for a minimum of 8 hours a day for three months postoperatively.

No Intervention: Standard postoperative care

Patients following bariatric surgery (RYGB or SG) will receive standard postoperative care.

Outcome Measures

Primary Outcome Measures

  1. Fat free mass retention [1 year]

    Fat free mass retention as measured using DEXA scan

  2. Weight loss [1 year]

    Weight loss (kg)

Secondary Outcome Measures

  1. Changes in protein and inflammatory marker levels [1 year]

    Change in myostatin, lipocalin-2, IGF-1, IL-6, testosterone

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Undergoing bariatric surgery- Roux en Y gastric bypass or sleeve gastrectomy Age 18-60 BMI >30kg/m2 Reporting regular physical exercise (>3 days/week) Willingness to comply with the study protocol
Exclusion Criteria:
  • Sedentary lifestyle Chronic pain that is constant and impairs the quality of life such as severe back, hip or knee pain Reduced mobility requiring the use of a mobility aid Undergoing revisional surgery Concerns from the investigator that the participant will be unable to fully comply with the study protocol

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University College Dublin

Investigators

  • Principal Investigator: Carel W le Roux, PhD, University College Dublin

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University College Dublin
ClinicalTrials.gov Identifier:
NCT04809129
Other Study ID Numbers:
  • RS20-012
First Posted:
Mar 22, 2021
Last Update Posted:
Mar 22, 2021
Last Verified:
Mar 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University College Dublin
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 22, 2021