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Study on Impact of Lifestyle Change and Weight Loss Before Bariatric Surgery (PREP)

Primary Purpose

Severe Obesity, Bariatric Surgery

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Preoperative lifestyle Intervention
Sponsored by
Duquesne University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Severe Obesity focused on measuring Morbid obesity, Diet therapy, Bariatric Surgery, Gastric bypass, Behavior therapy, Randomized controlled trial, Weight loss

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Any candidate for weight loss surgery who is at least 18 years old [At the University of Pittsburgh Medical Center, bariatric surgery is recommended as a treatment for individuals with Class III obesity (BMI > 40), or Class II obesity (BMI 35- 40) and serious obesity-related health problems]

Exclusion Criteria:

  • Mental retardation or psychosis
  • Previously diagnosed genetic obesity syndrome
  • Participation in a structured weight management program in the 6 months prior to study enrollment
  • Uncontrolled psychiatric symptomatology sufficiently severe to require immediate treatment
  • Pregnant or lactating in the previous 6 months
  • Taking a medication known to affect body weight such as oral steroids in the previous 6 months
  • Any previous surgery for weight loss
  • Deemed high risk surgical candidate.

Sites / Locations

  • Duquesne University

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

1

2

Arm Description

Usual preoperative care

Preoperative Lifestyle Intervention

Outcomes

Primary Outcome Measures

weight and related outcomes (BMI, cardiovascular risk, quality of life)
preparation for surgery (eating, activity and knowledge of surgery)
compliance and eating problems (vomiting, dumping, plugging etc.)
surgical complications and outpatient visits

Secondary Outcome Measures

Weight/BMI trajectory

Full Information

First Posted
February 14, 2008
Last Updated
March 15, 2016
Sponsor
Duquesne University
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT00623792
Brief Title
Study on Impact of Lifestyle Change and Weight Loss Before Bariatric Surgery
Acronym
PREP
Official Title
Preoperative Lifestyle Intervention in Bariatric Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
March 2008 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Duquesne University
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the trial is to determine whether a preoperative lifestyle intervention (targeting diet, exercise, and preparation for surgery) will favorably impact obesity-related parameters prior to bariatric surgery and improve short-term postoperative outcomes.
Detailed Description
This is a randomized, controlled trial to evaluate the impact of a preoperative lifestyle intervention that targets diet, exercise, and preparation for surgery as an adjunct to the surgical treatment of obesity. Patients will be randomized to a 6-month lifestyle intervention (n = 100) or to usual care (n = 100) prior to undergoing bariatric surgery. We aim to evaluate the effect of the intervention on select pre- and postoperative outcomes. We hypothesize that patients who participate in the preoperative intervention will exhibit greater improvements in weight and related outcomes and better preparation for surgery than those who receive usual care. After operation, we hypothesize that patients who participate in the intervention will exhibit better compliance and fewer behavior-related eating problems, as well as a lower rate of complications and fewer outpatient visits with surgery-related conditions than those who received usual preoperative care. Our secondary aim is to determine whether the intervention affects weight/BMI trajectory through 24 months after operation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Obesity, Bariatric Surgery
Keywords
Morbid obesity, Diet therapy, Bariatric Surgery, Gastric bypass, Behavior therapy, Randomized controlled trial, Weight loss

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
300 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
No Intervention
Arm Description
Usual preoperative care
Arm Title
2
Arm Type
Experimental
Arm Description
Preoperative Lifestyle Intervention
Intervention Type
Behavioral
Intervention Name(s)
Preoperative lifestyle Intervention
Intervention Description
6 month individual intervention consisting of weekly face-to-face and telephone sessions addressing diet, activity and preparation for surgery, followed by 3 "booster" telephone calls after surgery
Primary Outcome Measure Information:
Title
weight and related outcomes (BMI, cardiovascular risk, quality of life)
Time Frame
pre and post intervention
Title
preparation for surgery (eating, activity and knowledge of surgery)
Time Frame
pre and post intervention
Title
compliance and eating problems (vomiting, dumping, plugging etc.)
Time Frame
6- and 12-months post surgery
Title
surgical complications and outpatient visits
Time Frame
6- and 12-months post surgery
Secondary Outcome Measure Information:
Title
Weight/BMI trajectory
Time Frame
pre- and post-intervention; 6-, 12 and 24 months postop

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Any candidate for weight loss surgery who is at least 18 years old [At the University of Pittsburgh Medical Center, bariatric surgery is recommended as a treatment for individuals with Class III obesity (BMI > 40), or Class II obesity (BMI 35- 40) and serious obesity-related health problems] Exclusion Criteria: Mental retardation or psychosis Previously diagnosed genetic obesity syndrome Participation in a structured weight management program in the 6 months prior to study enrollment Uncontrolled psychiatric symptomatology sufficiently severe to require immediate treatment Pregnant or lactating in the previous 6 months Taking a medication known to affect body weight such as oral steroids in the previous 6 months Any previous surgery for weight loss Deemed high risk surgical candidate.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Melissa A Kalarchian, PhD
Organizational Affiliation
Duquesne University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Duquesne University
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15282
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
25443069
Citation
Kalarchian MA, Marcus MD, Courcoulas AP, Cheng Y, Levine MD. Self-report of gastrointestinal side effects after bariatric surgery. Surg Obes Relat Dis. 2014 Nov-Dec;10(6):1202-7. doi: 10.1016/j.soard.2014.08.007. Epub 2014 Aug 23.
Results Reference
derived

Learn more about this trial

Study on Impact of Lifestyle Change and Weight Loss Before Bariatric Surgery

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