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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01238354
Other study ID # RSSO-2010/2
Secondary ID
Status Completed
Phase N/A
First received November 9, 2010
Last updated June 14, 2016
Start date November 2010
Est. completion date December 2014

Study information

Verified date June 2016
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority Norway: Ethics Committee
Study type Interventional

Clinical Trial Summary

This study focuses on the difficulties to maintain a weight loss and behavioural change after having been in a institutional intermittent weight loss programme.

We explore if including a member of the family or a close friend in the treatment influences weight loss maintenance after completion of the programme.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Morbid obesity

- 18-50 years of age

- Having a relative or close friend who is willing to participate

Exclusion Criteria:

- Pregnancy

- Serious mental illness

- Severe overeating behaviour

- Significant reduced physical functioning

- Having undergone bariatric surgery earlier

- Serious heart disease

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Behavioral:
With friend

Without friend


Locations

Country Name City State
Norway Roros Rehabiliteringssenter Roros

Sponsors (1)

Lead Sponsor Collaborator
Norwegian University of Science and Technology

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Maintenance of weight loss 2 years after termination of programme No
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