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Effects of Self-conditioning Techniques in Promoting Weight Loss in Patients With Obesity. A Randomized Controlled Trial

Effects of Self-conditioning Techniques in Promoting Weight Loss in Patients With Severe Obesity. A Randomized Controlled Trial

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02978105
Enrollment
120
Registered
2016-11-30
Start date
2015-02-28
Completion date
2017-09-30
Last updated
2018-01-24

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

Conditions

Obesity

Brief summary

The investigators hypothesized that hypnosis is an alternative technique that could be applied to help patients with obesity to lose weight. The possibility that a self-conditioning technique (self-hypnosis) added to traditional approach (diet, exercise and behavioral recommendations) will be effective in determining weight loss with respect to the traditional approach in subjects with a body mass index (BMI) between 35 and 50 kg/m2 will be studied.

Detailed description

Obesity is a serious health concern. Most lifestyle interventions fail over time; indeed, overeating often involves loss of control and compulsive behaviors. Hypnosis could increase the ability to control emotional impulses. Self-conditioning techniques borrowed from hypnosis (self-hypnosis) increase self-control and self-management of emotions. Recent hypnosis techniques with a rapid-induction phase allow the trained patients to go into self-hypnosis in a few minutes and to repeat the experience in complete autonomy, employing a short time of the day only.

Interventions

OTHERself-conditioning techniques

Self-hypnosis to increase self-control before meals and every food compulsion episode

OTHERstandard care (diet, exercise and behavioral therapy)

dietary recommendations, exercise recommendations, and behavioral recommendations

Sponsors

University of Turin, Italy
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Able to give written informed consent * BMI between 35 and 50 kg/m2 * Age 20-70 years

Exclusion criteria

* Current or previous mental disorders and/or on any psychotropic drug * Insulin treatment * Candidates for bariatric surgery * Current (or discontinued for less than 6 months) treatment with anti-obesity drugs * Patients at risk of heart failure, edema, ascites (heart diseases, chronic liver diseases, nephrotic syndrome, renal failure) * Patients with untreated or uncompensated thyroid diseases

Design outcomes

Primary

MeasureTime frame
weight loss12 months after randomization

Secondary

MeasureTime frameDescription
Change in body fat percentage12 months after randomizationDual Energy X-Ray Absorptiometry (DEXA)
Change in fasting glucose12 months after randomization
Change in insulin circulating values12 months after randomization
Change in quality of life12 months after randomizationEuroQol (EQ)-5D \[Index and Visual Analog Scale (VAS)

Countries

Italy

Outcome results

None listed

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