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The Effect of CBT- Based Weight Loss Program on Obesity

The Effect of CBT- Based Weight Loss Program on Eating Behavior, Weight Loss Result and Risk for Coronary Heart Diseases and Type 2 Diabetes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01606904
Acronym
CognObe
Enrollment
62
Registered
2012-05-28
Start date
2012-05-31
Completion date
2016-03-31
Last updated
2018-05-11

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

Conditions

Anhedonia, Diabetes Mellitus, Type 2, Hypercholesterolemia, Obesity

Brief summary

The investigators purpose is to study how CBT (cognitive behavioral therapy)-based weight loss program affects on eating behavior, weight loss and risk factors for CHD (coronary heart diseases)and type 2 diabetes. Moreover, the investigators aim is to recognize subjects suffering from anhedonia (one of the core symptoms of depression, lack of pleasure) and follow how they benefit from the program in order to achieve maintained weight loss. Also, the associations between weight loss, physical activity and musculoskeletal disorders are studied.

Detailed description

Obesity is an increasing problem and effective weight loss methods are needed. The study is randomized follow-up study with 9 months intervention and three (3) years follow-up period. The study is organized in Oulu University Hospital, Department of Internal Medicine. Eighty (80)obese, 20-65 years, study subjects will be randomized into intervention or control group. The hypothesis of the CognObe study is: CBT (cognitive behavioral therapy)-based weight loss program is successful in sustained and favourable change in eating behavior and weight as well as decreased risk for coronary heart diseases or type 2 diabetes.

Interventions

BEHAVIORALCognitive behavioral therapy -based weight loss program

CBT-based program includes 20 group visits

Sponsors

Juho Vainio Foundation
CollaboratorOTHER
Yrjo Jahnsson Foundation
CollaboratorOTHER
Oulu University Hospital
CollaboratorOTHER
University of Oulu
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* BMI \> 30

Exclusion criteria

* other concurrent weight loss programs * disease which prevents weight loss * medication which affects on weight loss

Design outcomes

Primary

MeasureTime frameDescription
change in weightbaseline, 9 months, 1,2 and 3 yearskilograms

Secondary

MeasureTime frameDescription
change in eating behaviorbaseline, 9 months, 1,2 and 3 yearsemotional eating, uncontrolled eating, cognitive restraint, binge eating symptoms
change in total cholesterol,HDL, LDL,Trigly and glucosebaseline, 1,2 and 3 yearschange in laboratory values
DNAbaselinefor genetic analyses
change in incretinsbaseline, 12, 24 and 36 monthschange in incretins

Countries

Finland

Outcome results

None listed

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