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Efficacy of a Mobile Application to Help in Weight Loss Before Bariatric Surgery (VAMOS)

Primary Purpose

Morbid Obesity, Weight Loss

Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Care for today Mobile Application
Sponsored by
Hospital Universitari de Bellvitge
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Morbid Obesity focused on measuring Mobile APP, Obesity, R-en-Y gastric bypass, Preoperative weight loss

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients older than 18 and younger than 65 years who meet criteria to undergo bariatric surgery

BMI between 35 and 50 kg/m2 and indication of one-time surgery

Signing the informed consent of the study

Patient suitable for laparoscopic surgery

Patient who demonstrates accessibility to a smartphone and basic digital competence

Exclusion Criteria:

  • Previous bariatric surgery

Two-step surgery

Patient without resources to access the use of a Smartphone or without basic digital competence

Contraindication for surgery

Other surgical procedures associated with the same intervention

Sites / Locations

  • Hospital Universitari de BellvitgeRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

APP group

Normal VLCD (Very Low Calory Diet) group

Arm Description

Four months before surgery, the C4T APP, in addition to standard protocol, will be provided to all the patients randomized in the APP group.

Normal preoperative standard protocol will be provided to all the patients randomized in the normal group.

Outcomes

Primary Outcome Measures

Preoperative weight loss
To compare patients' preoperative weight loss after using the C4T APP versus the standard preoperative protocol.

Secondary Outcome Measures

patient information using the APP
A validated questionnaire will be used to compare patients' information using the APP vs. standard protocol. (10 questions, 1 point each: >6 good information achieved).
patient satisfaction using the APP
A validated questionnaire (will be used to compare patients' satisfaction using the APP vs. standard protocol. (10 items to evaluate as very poor, poor, correct, good, excellent).
Correlation between preoperative weight loss and early complications
Compare complications in the immediate postoperative period (30- and 90-days post-intervention) after the preoperative use of APP vs. standard protocol. Complications will be recorded in our prospective database.
Correlation between preoperative weight loss and Early postoperative weight loss
Compare patients' weight loss 3 months after surgery using the APP vs. standard protocol

Full Information

First Posted
September 23, 2022
Last Updated
December 15, 2022
Sponsor
Hospital Universitari de Bellvitge
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1. Study Identification

Unique Protocol Identification Number
NCT05598840
Brief Title
Efficacy of a Mobile Application to Help in Weight Loss Before Bariatric Surgery
Acronym
VAMOS
Official Title
Randomized Clinical Trial to Assess the Efficacy of a Mobile Application to Help in Weight Loss Before Bariatric Surgery: the VAMOS Project (Virtual Accompaniment for Morbid Obesity Surgery)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 18, 2022 (Actual)
Primary Completion Date
November 1, 2024 (Anticipated)
Study Completion Date
February 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitari de Bellvitge

4. Oversight

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

5. Study Description

Brief Summary
The present randomized clinical trial aims to prove the safety and efficacy of an interactive mobile application (Care4Today®) to obtain sufficient weight loss and empower patients with morbid obesity before being submitted to a gastric by-pass.
Detailed Description
Morbid obesity is considered the great epidemic of our century. It is regarded as the first non-traumatic cause of death in the western population and it is also progressively beginning to affect developing countries. The latest epidemiological studies estimate that in Spain more than 15% of the population has overweight and about 5% has morbid obesity. Obesity treatment is multidisciplinary, from lifestyle and dietary changes to surgery. Amongst the different available treatments, bariatric surgery is the only cost-effective in patients with morbid obesity. Bariatric surgery provides better results compared to both pharmacological treatments (which are less available and less effective) and lifestyle changes. Furthermore, as well as weight loss, it guarantees a better control of comorbidities, reducing the risk of cardiovascular disease, morbidity and mortality, improving quality of life. Although surgery is the best treatment option, patient commitment is necessary to achieve satisfactory results. Obtaining patient's comprehension of the importance of healthy lifestyle and equilibrated diet alongside with surgical information is generally difficult. Patient's concern needs to be constantly stressed out. The ongoing protocols that include preoperative meetings with surgeons, endocrinologists and nutritionists have been proved as insufficient, especially during the Covid-19 pandemic, when presential visits were reduced or cancelled. Preoperative optimization with a healthy lifestyle and a balanced diet few months before surgery potentially reduce intraoperative complications alongside with postoperative morbidity and mortality. Level of physical activity, diet and psychological stability could affect surgery's outcome for example reducing liver volume (up to 20%) and mesenteric fat. Also, an improvement in patient's preoperative satisfaction, anxiety and commitment to surgery have been suggested. Their impact on postoperative outcomes is unclear. There is lack of consensus on a standardized preoperative approach and goals. Many health care professionals worldwide strongly believe that preoperative optimization has an important impact on postoperative outcomes, but the evidence supporting this belief is mixed and most often retrospective. Although a positive relationship between self-monitoring behaviors (such as daily food intake diaries and regular self-weighing) and weight loss has been proved, additional instruction and behavioral intervention are needed. Besides weight loss, other factors such as adherence to self-monitoring of weight, recording food intake, increased physical activity could influence postoperative outcomes. Even though official guidelines for an enhanced recovery (ERAS, Enhanced Recovery After Surgery) in bariatric surgery recommend patient information, education, counseling and preoperative weight loss, the efficacy of these measures has not been proved. Technological development is an important resource that could help improving communications between patients and health care professionals. Nowadays, the use of a smartphone is widely integrated in daily life of most people. The number of smartphones used is constantly increasing every year. In 2016, there were more than seven billion users worldwide. The worldwide fast widespread of mobile technology in the last 15 years led to an expansion of the applications (APP) market. To date, the biggest APP market are 'Google Play' (Android), 'App store' (Apple) and 'Blackberry World' (Blackberry). This technological revolution has progressively affected the health world. An increasing number of medical APP have been designed in the last years, few directly managed from health care providers from public or private centers. The Mobile Health APP could led to a simpler, real-time connection between patients and health care professionals alongside with a bidirectional data flow and a steadily monitorization of patients' evolution that could obtain a better preoperative follow-up without increasing the costs. The present randomized clinical trial aims to prove the safety and efficacy of an interactive mobile application (Care4Today®) to obtain sufficient weight loss and empower patients with morbid obesity before being submitted to a gastric by-pass.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Morbid Obesity, Weight Loss
Keywords
Mobile APP, Obesity, R-en-Y gastric bypass, Preoperative weight loss

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
APP group
Arm Type
Experimental
Arm Description
Four months before surgery, the C4T APP, in addition to standard protocol, will be provided to all the patients randomized in the APP group.
Arm Title
Normal VLCD (Very Low Calory Diet) group
Arm Type
Active Comparator
Arm Description
Normal preoperative standard protocol will be provided to all the patients randomized in the normal group.
Intervention Type
Other
Intervention Name(s)
Care for today Mobile Application
Intervention Description
C4T (Care for Today) Education is a digital application (app) designed to offer quality educational materials. The APP will be provided to the patients in the outpatient centre four months before surgery. Patients will be able to download the APP using a QR code that will be provided during the visit. They'll realize the download immediately or at home, in both cases a detailed explication of how to use the APP and its contents will be provided using an example version.
Primary Outcome Measure Information:
Title
Preoperative weight loss
Description
To compare patients' preoperative weight loss after using the C4T APP versus the standard preoperative protocol.
Time Frame
App will be provided four months before surgery and then preoperative weight loss achieved will be evaluated the day of surgery
Secondary Outcome Measure Information:
Title
patient information using the APP
Description
A validated questionnaire will be used to compare patients' information using the APP vs. standard protocol. (10 questions, 1 point each: >6 good information achieved).
Time Frame
App will be provided four months before surgery and patients' information/satisfaction using the APP will be evaluated the day of surgery
Title
patient satisfaction using the APP
Description
A validated questionnaire (will be used to compare patients' satisfaction using the APP vs. standard protocol. (10 items to evaluate as very poor, poor, correct, good, excellent).
Time Frame
App will be provided four months before surgery and patients' information/satisfaction using the APP will be evaluated the day of surgery
Title
Correlation between preoperative weight loss and early complications
Description
Compare complications in the immediate postoperative period (30- and 90-days post-intervention) after the preoperative use of APP vs. standard protocol. Complications will be recorded in our prospective database.
Time Frame
Early complication rate in each group will be evaluated and compared 30 and 90 days postoperative
Title
Correlation between preoperative weight loss and Early postoperative weight loss
Description
Compare patients' weight loss 3 months after surgery using the APP vs. standard protocol
Time Frame
Patients' weight loss in each group will be evaluated and compared 3 months after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients older than 18 and younger than 65 years who meet criteria to undergo bariatric surgery BMI between 35 and 50 kg/m2 and indication of one-time surgery Signing the informed consent of the study Patient suitable for laparoscopic surgery Patient who demonstrates accessibility to a smartphone and basic digital competence Exclusion Criteria: Previous bariatric surgery Two-step surgery Patient without resources to access the use of a Smartphone or without basic digital competence Contraindication for surgery Other surgical procedures associated with the same intervention
Facility Information:
Facility Name
Hospital Universitari de Bellvitge
City
L'Hospitalet De Llobregat
State/Province
Barcelona
ZIP/Postal Code
08907
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Javier Osorio, MD, PhD
Phone
932 60 75 00
Email
javier_osorio2003@yahoo.es

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Efficacy of a Mobile Application to Help in Weight Loss Before Bariatric Surgery

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