BePATIENT: Assessing the Value of eHealth for Bariatric Surgery

Sponsor
Catharina Ziekenhuis Eindhoven (Other)
Overall Status
Unknown status
CT.gov ID
NCT03394638
Collaborator
(none)
200
1
3
33.7
5.9

Study Details

Study Description

Brief Summary

Bariatric surgery is the only treatment with long standing effect of morbid obesity. The key elements to success are the patient-selection, an experienced bariatric team and a completed follow-up program. Follow-up programs can consist of, for example, providing social support in support groups, teaching psychological skills, such as coping with the body change or teaching self-regulation of body weight. Furthermore, follow-up is important for dietary and sports counselling. The experience of the team members and coaching skills are essential in indicating the suitable procedure if necessary and guide the patients through the process. Various studies showed a significant positive effect of a completed follow-up program after bariatric surgery on maintaining weight loss. There is a burden for this on site provided care as organizational and financial resources are not unlimited. Especially as the follow-up period is an obligatory 5 years or if possible life long. Even if this aftercare is provided, not all patients complete the complete program. Various reasons are possible for an increasing no-show-rate, the loss of enthusiasm for onsite visits could be one of them. Analogue to other chronic diseases, the addition of telehealth could be useful. Telehealth is the delivery of health-related services and information via telecommunications technologies. It encompasses preventative, promotive and curative aspects. Examples are exchanging health services or education via videoconference, transmission of medical data for disease management (remote monitoring) and advice on prevention of diseases and promotion of good health by patient monitoring and follow-up. The participation of eHealth has been investigated and considered useful in the treatment of obesity. In a systematic review self-measured blood pressure monitoring was associated with better control of hypertension at least in the first year. Its value in a bariatric tract has not been investigated. It can be hypothesized that self-control by eHealth could enhance clinical outcome as more weight loss and comorbidity reduction. Long-term realistic goals setting, consistent use of routines and self-monitoring has been proven effective for weight loss maintenance. Patients with higher self-control are more certain regarding their abilities, which cause higher commitment and adherence to the program. This eventually leads to more weight loss. For this purpose an online monitoring program was designed for our Obesity Centre (BePATIENT) to provide preoperative information as well as aids in the post-bariatric phase by self-control wireless devices for registration of biometric outcomes, teleconference opportunities and access to additional information. In a prospective trial the implementation in several degrees is evaluated.

Condition or Disease Intervention/Treatment Phase
  • Other: Access to online eLearning module
  • Other: Access to measurement devices
  • Procedure: Conventional group
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Assessing the Value of eHealth for Bariatric Surgery
Actual Study Start Date :
Feb 21, 2017
Anticipated Primary Completion Date :
Dec 15, 2019
Anticipated Study Completion Date :
Dec 15, 2019

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Conventional group

Treatment includes: 10 individual and 3 group consultations at the outpatient department by several disciplines in the first postoperative year. Additional visits if necessary No further access to the BePATIENT website

Procedure: Conventional group
All patients undergo the standard of care which included: the bariatric procedure and several outpatient visits including consultation with their surgeon, obesity nurses, dieticians and (if indicated) psychologists.

Experimental: Online group

Treatment includes: Added to conventional group: Continuation of access to the BePATIENT website with: eLearning programs Informative videos Patient network Video consulting

Other: Access to online eLearning module
Patients enrolled in the Online group have access to an online platform called BePatient. Patients are given the ability to access the platform and do eLearnings; watch videos about the operation and recovery; do quizzes, see dietary advices; see news about obesity and our department; read patients' stories. They are also able to chat with other patients.

Procedure: Conventional group
All patients undergo the standard of care which included: the bariatric procedure and several outpatient visits including consultation with their surgeon, obesity nurses, dieticians and (if indicated) psychologists.

Experimental: Device group

Added to Online group:Four wireless devices, which are Weight Scale Blood Pressure Oximeter Activity Tracker

Other: Access to online eLearning module
Patients enrolled in the Online group have access to an online platform called BePatient. Patients are given the ability to access the platform and do eLearnings; watch videos about the operation and recovery; do quizzes, see dietary advices; see news about obesity and our department; read patients' stories. They are also able to chat with other patients.

Other: Access to measurement devices
Patients in the device group have, in addition to patients in the Online group, access to 4 measuring devices, including: weight scale, oximeter, activity bracelet and blood pressure device. Those devices are connectable to their mobile phones where patients can view their own progress.

Procedure: Conventional group
All patients undergo the standard of care which included: the bariatric procedure and several outpatient visits including consultation with their surgeon, obesity nurses, dieticians and (if indicated) psychologists.

Outcome Measures

Primary Outcome Measures

  1. Body Mass Index (BMI) [2 years after the operation]

    The BMI in kg/m2 at 2 years postoperatively.

Secondary Outcome Measures

  1. Quality of Life [At 1 and 2 years after the operation]

    Quality of Life assessment using the RAND36-questionnaire. The RAND36 questionnaire consists of 36 questions about health related quality of life. The RAND36 scores are divided in 9 subscales: vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning, mental health and health change. Scores for each subscale are transformed to a linear 0 - 100 score. A higher score indicates a better quality of life in that domain.

  2. Evolution of obesity related comorbidities [At 1 and 2 years after the operation]

    Status of comorbidities are recorded at 1 and 2 years postoperatively and classified as either: cured (no medication and no complaints), improved (less medication needed and/or less complaints), unchanged (no alterations in medication use and no change in complaints), worsened (more medication needed and/or more complaints) or de novo (development of a comorbidity which was not present at inclusion). The reviewed comorbidities include: hypertension, diabetes mellitus, Arthralgia, obstructive sleep apnea syndrome, dyslipidemia and gastro-esophageal reflux disease.

  3. Program commitment [At 1 and 2 years after the operation]

    A 6-item questionnaire to assess program commitment (Neubert & Cady 2001).

  4. Technical errors biometric devices [At 2 years after the operation]

    Number of technical issues reported by patients or health care professionals

  5. Length of hospitalization [At 2 years after the operation]

    Length of stay in hospital (days)

  6. Return to work (days) [At 1 year after the operation.]

    Number of days patients start working again after operation

  7. Patients' satisfaction [At 1 and 2 years after the operation]

    Satisfactory assessment patients (Numeric Rate Scale 0-10)

  8. Health care suppliers' satisfaction [At 1 and 2 years after the operation]

    Satisfactory assessment health care professional (Numeric Rate Scale 0-10)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Completed the questionnaire online

  2. Having ongoing access to internet

  3. Ability to use a model of mobile device (smartphone or tablet) with any version of the Android or iOS platform

  4. A body mass index above 40 kg/m2 or above 35 kg/m2 with related comorbidity (hypertension, diabetes type 2, hyperlipidaemia, obstructive sleep apnea syndrome or joint arthritis of lower limbs)

  5. A primary gastric sleeve or bypass planned

  6. Age of 18 years or more

  7. Ability to read and write the Dutch language

  8. Signed informed consent

Exclusion Criteria:
  1. Patients not meeting the inclusion criteria

Contacts and Locations

Locations

Site City State Country Postal Code
1 Catharina Hospital Eindhoven Noord Brabant Netherlands 5623EJ

Sponsors and Collaborators

  • Catharina Ziekenhuis Eindhoven

Investigators

  • Principal Investigator: Simon Nienhuijs, MD, PhD, Department of Surgery, Catharina Hospital Eindhoven

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dirk Versteegden, MD, Catharina Ziekenhuis Eindhoven
ClinicalTrials.gov Identifier:
NCT03394638
Other Study ID Numbers:
  • NL56992.100.16
First Posted:
Jan 9, 2018
Last Update Posted:
Jan 11, 2018
Last Verified:
Jan 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dirk Versteegden, MD, Catharina Ziekenhuis Eindhoven
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 11, 2018