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Effects of Body Contouring Surgery in Obese Patients

Effects of Body Contouring Surgery in Obese Patients: a Prospective Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02532751
Enrollment
100
Registered
2015-08-26
Start date
2018-04-30
Completion date
2021-12-31
Last updated
2018-02-22

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

Conditions

Quality of Life, Validation Study

Brief summary

The aim of this study is twofold; 1) to assess the psychometric properties of the Finnish version of the BODY-Q questionnaire, 2) to assess the effects of body contouring surgery using patient-reported outcome measures.

Detailed description

The BODY-Q is translated into Finnish through forward and backward translation and a committee review. The preliminary version is pilot tested with 20 participants undergoing body contouring surgery. The study is of longitudinal design gathering data from participants undergoing body contouring surgery due to obesity. Data collection takes place in the Department of Plastic Surgery, Helsinki University Central Hospital, Helsinki, Finland. The participants fill in three patient-reported outcome measures. The outcomes of the three patient-reported outcome measures are compared with each other and internal validity assessed. Test-retest reliability is assessed after two weeks from the first completion of the questionnaires. With validated questionnaires the effects of body contouring surgery is assessed.

Interventions

None listed

Sponsors

Helsinki University Central Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Body contouring surgery due to: A) massive weight loss B) Postbariatric weight loss * Patient age over 18 years

Exclusion criteria

* Patient age under 18 years * No body contouring surgery * Surgical intervention performed in another hospital than Helsinki and Uusimaa Hospital District * No obesity

Design outcomes

Primary

MeasureTime frameDescription
Validity of the Finnish version of the BODY-Q questionnaire6 monthsThe psychometric properties of the BODY-Q patient-reported outcome measure are measured
Health-related quality of life after body contouring surgery in obese patients0.5 to 3 yearsHealth-related quality of life is assessed with a questionnaire
Depression after body contouring surgery in obese patients0.5 to 3 yearsDepression is assessed with a questionnaire
Body image after body contouring surgery in obese patients0.5 to 3 yearsBody image is assessed with a questionnaire

Secondary

MeasureTime frameDescription
The BODY-Q questionnaire0.5 to 3 yearsAssessment of health-related quality of life and body image
The Raitasalo Beck Depression Index questionnaire0.5 to 3 yearsAssessment of depression
The 15-Dimensions health-related quality of life instrument0.5 to 3 yearsAssessment of health-related quality of life

Countries

Finland

Contacts

Primary ContactJussi P Repo, MD
mrjussirepo@gmail.com+358443593100
Backup ContactPentscho Popov, MD, PhD
pentscho.popov@hus.fi+35894711

Outcome results

None listed

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