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Effects of Body Contouring Surgery in Obese Patients

H

Helsinki University Central Hospital (HUCH)

Status

Unknown

Conditions

Quality of Life
Validation Study

Study type

Observational

Funder types

Other

Identifiers

NCT02532751
204/13/03/02/15/1

Details and patient eligibility

About

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.

Full 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.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

2

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Central trial contact

Jussi P Repo, MD; Pentscho Popov, MD, PhD

Data sourced from clinicaltrials.gov

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