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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02000037
Other study ID # 2013-A00800-45
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date October 18, 2013
Est. completion date January 28, 2016

Study information

Verified date December 2022
Source Institut Pasteur de Lille
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aim is to Assess the Effect of an IR Reflexotherapy on Overweight and Class I Obese People.


Recruitment information / eligibility

Status Terminated
Enrollment 87
Est. completion date January 28, 2016
Est. primary completion date January 28, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 60 Years
Eligibility Inclusion Criteria: - BMI between 27 and 35 kg/m2 (included), - Aged 30 to 60 years old (included), - Stable weight: no variation of 3 kg in the las 3 months, - Signed the consent form, - Able to follow the study, - Health insured. Exclusion Criteria: - History of coronary disease (in the last 6 months), - Progressive illness at the time of the study (cancer, neurodegenerative disease...), - Diabetics (treated or not), - Fasting blood total cholesterol equal or over 2.5 g/L (treated or not), - Fasting blood triglycerides equal or over 2.0 g/L (treated or not), - Fasting blood glucose equal or over 1.26 g/L, - Peripheral neuropathy (polyneuritis, diabetic neuropathy) or central neuropathy (hemiplegia), - Infectious cutaneous condition or allergies (to the contact point of the device), - History of stroke, - Severe heart disease, - Epilepsy, - Reduced motility, - Diagnosed eating disorder, - Followed a diet in the last 90 days in order to lose weight, - Took weight loss assistance drug (Orlistat) in the last month or is likely to take one during the study, - Psychiatric disorder incompatible with the study, - Mental illness, - Neurological disorder, - Chronic somatic disease, - Addiction or nicotine withdrawal, - Under psychoactive drug , - Alcool consumption over 3 glasses a day, - Pregnant or breastfeeding women, - Women that are likely to get pregnant during the study, - Is unable to understand or follow the protocol - Is deprived of liberty - Is under judicial protection

Study Design


Related Conditions & MeSH terms

  • Assess the Effect of an IR Reflexotherapy on Overweight and Class I Obese People
  • Overweight

Intervention

Device:
IR Reflexotherapy
18 IR reflexotherapy sessions : Once a week for 12 weeks at the beginning of the study Once a week for 3 weeks, 9 months after the beginning of the study Once a week for 3 weeks, 15 months after the beginning of the study
Behavioral:
Dietary care
Dietary consultation 1, 2, 3, 6, 9, 12, 15 and 18 months after the beginning of the study

Locations

Country Name City State
France NutrInvest - Institut Pasteur de Lille Lille Nord

Sponsors (2)

Lead Sponsor Collaborator
Institut Pasteur de Lille Luxomed

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Weight changes after 12 months compared to a dietary care (associated with physical activity advice) dispensed by a professional. 12 months
Secondary Effect of infrared (IR) reflexotherapy on weight changes. 3, 12 and 18 months
Secondary Effect of IR reflexotherapy combined with a dietary care (and physical activity advises) dispensed by a professional on the weight changes. 3, 12 and 18 months.
Secondary Effect of infrared (IR) reflexotherapy on waist size. 3, 12 and 18 months
Secondary Effect of IR reflexotherapy combined with a dietary care (and physical activity advises) dispensed by a professional on the waist siez. 3, 12 and 18 months.
Secondary Effect of infrared (IR) reflexotherapy on dietary habits. 3, 12 and 18 months
Secondary Effect of IR reflexotherapy combined with a dietary care (and physical activity advises) dispensed by a professional on dietary habits. 3, 12 and 18 months.
Secondary Effect of infrared (IR) reflexotherapy on life's quality (anxiety, depression, physical impact, psychosocial, impact on sexual life, eating well-being, feeling about the dietary care). 3, 12 and 18 months
Secondary Effect of IR reflexotherapy combined with dietary care (and physical activity advises) dispensed by professional on life quality (anxiety, depression, physical impact, psychosocial, impact on sexual life, eating wellbeing, feeling about the dietary care) 3, 12 and 18 months.
Secondary Effect of infrared (IR) reflexotherapy on the salivary cortisol. 3 months
Secondary Effect of IR reflexotherapy combined with a dietary care (and physical activity advises) dispensed by a professional on the salivary cortisol. 3 months.
Secondary Effect of infrared (IR) reflexotherapy on blood pressure and heart rate. 3 months
Secondary Effect of IR reflexotherapy combined with a dietary care (and physical activity advises) dispensed by a professional on blood pressure and heart rate. 3 months.