Trial · NCT03431831

Assessment of and Treatment Applied to Food Addiction in a Rural Healthy Behaviors Clinic

NCT03431831, Phase 4, Completed, University of Nebraska; results first posted 2024-08-29

3 sourcestrials-2026-11-12-0.5.0

Cite this record

ConductScience Library. Assessment of and Treatment Applied to Food Addiction in a Rural Healthy Behaviors Clinic. Trials, record NCT03431831. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03431831

On this page

Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title: Assessment of and Treatment Applied to Food Addiction in a Rural Healthy Behaviors Clinic
NCT number: NCT03431831
Status: Completed
Phases: Phase 4
Enrollment: 86 participants, actual
Lead sponsor: University of Nebraska
Conditions: Obesity
Interventions: Intervention Control, Counselling, Contrave, Contrave and Counseling
First posted: 2018-02-13
Last updated: 2024-08-29
Results first posted: 2024-08-29

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

List	Outcome	Time frame	Description
Primary	Weight	difference between baseline and 6 months	Weight in lbs
Primary	Body Mass Index (BMI)	difference between baseline and 6 months	Body Mass Index (BMI): Underweight Below 18.5, Normal 18.5-24.9, Overweight 25.0-29.9, Obesity 30.0 and Above

Source ClinicalTrials.gov

Outcomes2

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

Type	Outcome	Time frame	Population	Units	Measured as
PRIMARY	Weight	difference between baseline and 6 months	difference between first and last weight measure among each group	lbs	MEAN
PRIMARY	Body Mass Index (BMI)	difference between baseline and 6 months	difference between first and last BMI measure among each group	kg/m2	MEAN

Source ClinicalTrials.gov

Results by group16

Each measurement the trial posted, group by group, in the words and numbers it posted.

Outcome	Group	Value	Spread	Units
Weight	FA+ Intervention Control	-2.08	Full Range -8.7 to 4.7	lbs
Weight	FA+ Counselling	-3.42	Full Range -10.6 to 3.2	lbs
Weight	FA+ Contrave	-4.36	Full Range -7.5 to 3.6	lbs
Weight	FA+ Contrave and Counseling	-2.4	Full Range -10.4 to 4.4	lbs
Weight	FA- Intervention Control	-0.2	Full Range -7.1 to 5.9	lbs
Weight	FA- Counseling	-2.5	Full Range -9.1 to 4.3	lbs
Weight	FA-Contrave	-3.3	Full Range -9.6 to 1.8	lbs
Weight	FA- Contrave and Counseling	-2.74	Full Range -10.2 to 6.9	lbs
Body Mass Index (BMI)	FA+ Intervention Control	-0.87	Full Range -3.4 to 1.8	kg/m2
Body Mass Index (BMI)	FA+ Counselling	-1.36	Full Range -3.6 to 1	kg/m2

1 to 10 of 16Source ClinicalTrials.gov

See all 16 results by group

Participant flow24

How many started, completed or left each group, period by period.

Period	Milestone	Group	Participants
Overall Study	STARTED	FA+ Intervention Control	8
Overall Study	STARTED	FA+ Counselling	10
Overall Study	STARTED	FA+ Contrave	10
Overall Study	STARTED	FA+ Contrave and Counseling	10
Overall Study	STARTED	FA- Intervention Control	13
Overall Study	STARTED	FA- Counseling	14
Overall Study	STARTED	FA-Contrave	11
Overall Study	STARTED	FA- Contrave and Counseling	10
Overall Study	COMPLETED	FA+ Intervention Control	6
Overall Study	COMPLETED	FA+ Counselling	8

1 to 10 of 24Source ClinicalTrials.gov

See all 24 participant flow

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals24

The totals the trial posted for each group.

Total	Group	At risk
Total, all-cause mortality	Intervention Control/ FA-	13
Total, all-cause mortality	Counselling/ FA-	14
Total, all-cause mortality	Contrave/FA-	11
Total, all-cause mortality	Contrave and Counseling/FA-	10
Total, all-cause mortality	Intervention Control/FA +	8
Total, all-cause mortality	Counseling/FA+	10
Total, all-cause mortality	Contrave/FA+	10
Total, all-cause mortality	Contrave and Counseling/FA+	10
Total, other adverse events	Intervention Control/ FA-	13
Total, other adverse events	Counselling/ FA-	14

1 to 10 of 24Source ClinicalTrials.gov

See all 24 adverse event totals

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMID	Listed as
33389719	DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov: 2026-11-12; ClinicalTrials.gov
Results, from AACT: 2026-03-23; AACT
NIH grant links: 2026-11-13; NIH RePORTER

Sources 3

ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
ClinicalTrials.govNo license stated
NIH RePORTER's clinical studies and project filesPublic domain

Each source's terms

ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
ClinicalTrials.govnone stated
NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT03431831

GET https://conductscience.org/api/trials/v1/NCT03431831/flow?page=2

API reference For AI assistants