NCT00694811

CompletedPhase 4

Effects of Re-Feeding Duration on Weight Maintenance After W...

Göteborg University Source

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Other study identifiers

Sponsor study identifier

VGFOUREG-1942

Study Type

interventional

Actual enrollment (reported)

169

Locations

1 country

Sites

1

Timeline

Study Start

August 2004

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

January 2008

Actual (reported)

Study Completion

January 2008

Actual (reported)

Brief Summary

The primary objective of the study is to test the hypothesis that prolonged re-feeding after VLED induced weight loss improves weight maintenance and eating behaviour

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 169 participants
Study completion date: January 2008
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
August 2004
Date type not reported
This date has not been verified as actual or estimated.
Primary Completion
January 2008
Actual (reported)
Study Completion
January 2008
Actual (reported)
First Submitted
June 9, 2008
Actual (reported)
First Posted
June 11, 2008
Actual (reported)

Last Updated: June 11, 2008
Status Verified: June 2008
Last Update Submitted: June 10, 2008

Conditions

Obesity

Keywords

ObesityWeight lossDietVery-low-energy dietPredictive factorsRe-feeding

Outcome Measures

Primary Outcomes (1)

Weight development
52 weeks

Secondary Outcomes (1)

Eating behaviour (Three Factor Eating Questionnaire)
52 weeks

Study Arms (2)

A

EXPERIMENTAL

1 week of re-feeding

Behavioral: Re-feeding duration

B

EXPERIMENTAL

6 weeks of re-feeding

Behavioral: Re-feeding duration

Interventions

Re-feeding durationBehavioral

1 or 6 weeks of re-feeding after VLED-induced weight loss

Also known as: Dietary advice

AB

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years - 60 Years

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64)

You may qualify if:

age 18-60 years
BMI \> 30 kg/m2

Sponsors & Collaborators

Göteborg University
Otherlead

Study Sites (1)

Sahlgrenska University Hospital

Gothenburg, Sweden

MeSH Terms

Conditions

ObesityWeight Loss

Interventions

Nutrition Assessment

Condition Hierarchy (Ancestors)

OverweightOvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and SymptomsBody Weight Changes

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic Methods

Study Officials

Kaj Stenlöf, MD
Institute of Medicine, Sahlgrenska Academy, University of Gothenburg
STUDY CHAIR

Enrollment

169 participants (actual enrollment reported by the registry).

Study Design

Study Type: interventional
Phase: phase 4
Allocation: RANDOMIZED
Masking: NONE
Purpose: TREATMENT
Intervention Model: PARALLEL
Sponsor Type: OTHER

Study Record Dates

First Submitted

June 9, 2008

First Posted

June 11, 2008

Study Start

August 2004

Date type not reported

This date has not been verified as actual or estimated.

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speaking swedish

You may not qualify if:

eating disorder
unstable diabetes type 1
unstable cardiac disease
severe psychiatric disorder
pregnancy or lactation

Contact the study team to confirm eligibility.

Investigative Techniques

Health Care Evaluation Mechanisms

Quality of Health Care

Health Care Quality, Access, and Evaluation

Epidemiologic Measurements

Public Health

Environment and Public Health

Primary Completion

January 2008

Actual (reported)

Study Completion

January 2008

Actual (reported)

Last Updated

June 11, 2008

Record last verified: 2008-06

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT00694811
Data provider: ClinicalTrials.gov
Source updated: 2008-06-11
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:33:54 UTC

Locations

SE(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

Primary Completion

Study Completion

First Submitted

First Posted

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (2)

A

B

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Interventions

Condition Hierarchy (Ancestors)

Intervention Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations