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Preliminary Evaluation Study of Therapeutic Education on Overweight People in Addition to a Hydrotherapeutic Cure

Preliminary Evaluation Study of Therapeutic Education on Overweight People in Addition to a Hydrotherapeutic Cure at the Thermal Baths of Brides-les-Bains

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02284776
Acronym
Educatherm
Enrollment
400
Registered
2014-11-06
Start date
2013-07-31
Completion date
2016-04-30
Last updated
2015-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

Therapeutic education

Brief summary

The goal of this study is to assess the effect of a therapeutic education program in addition of a hydrotherapeutic cure on obese patients. The therapeutic education program at the thermal baths of Brides-les-Bains is composed of a dietary follow-up, a physical activities program, working group.

Detailed description

The participants are people that come to the thermal baths in order to follow an hydrotherapeutic cure (of about 3 weeks). For the Action group, they also follow a course of therapeutic education where they are given advices on how they should eat and have a regular physical activity. This therapeutic education in addition of the hydrotherapeutic cure should help them lose weight and not gain in again. The participants are followed for 18 months (17 months after leaving the thermal baths).

Interventions

BEHAVIORALTherapeutic education

People in hydrotherapeutic cure are following a program of Therapeutic Education. This program includes dietary advice, physical activities, behavior advice in order to change the lifestyle of the obese people.

Sponsors

Association Francaise pour la Recherche Thermale
CollaboratorOTHER
Société des Etablissements Thermaux de Brides-les-Bains et Salins-les-Bains
CollaboratorUNKNOWN
Centre d'Investigation Clinique 9301 INSERM-CHRU de Lille
CollaboratorUNKNOWN
Institut Pasteur de Lille
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Body Mass Index (BMI) over 27 kg/m² (or equal) * Has a valid email address, has access to the internet and to a telephone line * Has a domestic scale compatible with its weight * Signed the consent form * Susceptible to accept the obligations generated by the study * Has a health insurance

Exclusion criteria

* Has a progressive illness at the time of the study (cancer, neurodegenerative disease...) * Is pregnant * Follows the hydro-therapeutic cure in order to cure rheumatism * Trying to lose weight prior to a surgery * Has a diagnosed eating disorder * Has no physical activity due to a handicap or a serious osteoarthritis * Has taken a weight-loss drug (Orlistat) in the past month or will likely do so in the future * Is taking a Desmopressin-based drug * Is unable to understand or follow the protocol * Is deprived of liberty * Is under judicial protection

Design outcomes

Primary

MeasureTime frameDescription
Change in the weight between the end of the hydrotherapeutic cure and 5 months after the hydrotherapeutic curePeople's weight in between the end of hydrotherapeutic cure and 5 months after hydrotherapeutic curePeople weight themselves on a domestic scale.

Secondary

MeasureTime frameDescription
Quality of life0 ; 3 weeks ; 6 months ; 12 monthsAssessed with the Short SF-36 questionnaire.
Physical activity0 ; 3 weeks ; 6 months ; 12 monthsAssessed with the Ricci-Gagnon questionnaire.
Individual's readiness to change0 ; 3 weeks ; 6 months ; 12 monthsAssessed with the Prochaska questionnaire.
Evolution of the weight.0 ; 3 weeks ; 6 months ; 12 months ; 18 monthsPeople weight themselves on a domestic scale.
Felling about the body0 ; 3 weeks ; 6 months ; 12 monthsQuestionnaire on how the participants feel about their body.
Dietary habits0 ; 3 weeks ; 6 months ; 12 monthsQuestionnaire about the dietary habits of the participants.
Visual and analogical scale for general and psychological well-being and body discomfort.0 ; 3 weeks ; 6 months ; 12 monthsParticipants mark down on a 10cm scale how they feel.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026