Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
100 participants
OBSERVATIONAL
2018-04-30
2021-12-31
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
A) massive weight loss B) Postbariatric weight loss
* Patient age over 18 years
Exclusion Criteria
* No body contouring surgery
* Surgical intervention performed in another hospital than Helsinki and Uusimaa Hospital District
* No obesity
18 Years
ALL
No
Sponsors
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Helsinki University Central Hospital
OTHER
Responsible Party
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Jussi Repo
MD
Locations
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Jorvi Central Hospital
Espoo, Uusimaa, Finland
Helsinki University Central Hospital
Helsinki, Uusimaa, Finland
Countries
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Central Contacts
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Facility Contacts
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Tiina Jahkola, MD, PhD
Role: primary
Pauliina Homsy, MD, PhD (Cantab)
Role: backup
Other Identifiers
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204/13/03/02/15/1
Identifier Type: -
Identifier Source: org_study_id
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