Skip to main content
OpenTrials
Completed

NCT Number: NCT02374866

Monitoring Obese Patients : Impact on the Frequency of Monitoring Weight

The literature data show that long-term monitoring has an effect on weight loss, comorbidity and on improving the quality of life. However, there are still no studies on monitoring obese patients after taking initial multidisciplinary approach. The recommendations of the HAS 2011 advocated "continuous monitoring needed to prevent weight regain, monitor the consequences of overweight and treat comorbidities. This requires a long-term support. "The frequency of follow-up consultations is not specified and "must be adapted to achieve a weight loss target and maintain." Having no specific recommendations on the frequency of monitoring, the investigators chose to experiment closer monitoring than our current monitoring to assess what is the best frequency monitoring, in terms of: weight loss, quality of life, feeding behavior, changes in physical abilities, evolution of comorbidities associated with obesity. The recommendations of the HAS 2011 advocate support of a multidisciplinary obesity for weight loss of 5% to 10 %, which, if maintained, can reduce comorbidities associated with obesity (type 2 diabetes, hypertension, pain associated with osteoarthritis).

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Centre de suivi de l'obésite Bernard Descottes

Saint-Yrieix-la-Perche, 87500, France

About this study

2 groups of randomized patients will be followed:

  • The control group will follow the current center: every four months for a year, combined with monitoring by email or regular mail during the year.
  • The experimental group will be a follow-up every two months for one year HDJ more of the same followed by email or postal mail.

Follow by email or mail is identical to the control group, as well as HDJ 12 months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • - Age ≥ 18 - ≤ 75 years
  • Obesity with a BMI ≥ 35 or ≥ 30 if associated with at least one comorbidity whose support was commenced or continued during the initial hospitalization.
  • Patients hospitalized for a period of at least 3 weeks in the Bernard Descottes center and were supported on dietary, psychological, psychomotor and physical education in a therapeutic approach.
  • Patients who have signed consent form.
  • Patients who never underwent bariatric surgery and bariatric surgery have not seen in the year following their hospitalization in Bernard Descottes Center.
  • Patient accepting the constraints of the protocol in case of close monitoring.
  • Patients able to travel with their own vehicle to Bernard Descottes Center.
  • Affiliate or beneficiary of a social security scheme

Exclusion criteria

  • - Patients who have hospitalized in Bernard Descottes Center.
  • Failure to follow the protocol because of insufficient command of French or concomitant illness.
  • Pregnant or breastfeeding.
  • Patients under guardianship or under judicial protection.
  • Participation to another trial which can impact on patient's experimental disease during all the study, and patients who are in an exclusion period of another trial.

Treatment and study plan

closer monitoring

Other

Primary outcomes

  1. percentage of weight loss at 12 months

    Time frame: 1 year

  2. percentage of change in BMI at 12 months

    Time frame: 1 year

Secondary outcomes

  1. Change of waist at 12 months

    Time frame: 1 year

  2. Changes in body composition

    Time frame: 1 year

  3. Change of quality of life at 12 months

    Time frame: 1 year

  4. Change of medication at 12 months

    Time frame: 1 year

Sponsors and collaborators

Lead sponsor

University Hospital, Limoges

Other

Registry information

Official study title

Monitoring Obese Patients: Impact on the Frequency of Monitoring Weight, Quality of Life, Dietary Behavior, Physical Ability and Comorbidities

Acronym: SUIVIOBESITE

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Mar 2, 2015
Registry last updated
Sep 5, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.