NCT01506297

Brief Summary

Subjective measures of satiety are correlated with biologic mechanisms of appetite control.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
31

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jul 2012

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 3, 2012

Completed
6 days until next milestone

First Posted

Study publicly available on registry

January 9, 2012

Completed
6 months until next milestone

Study Start

First participant enrolled

July 1, 2012

Completed
2.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2014

Completed
Last Updated

August 3, 2018

Status Verified

August 1, 2018

Enrollment Period

2.1 years

First QC Date

January 3, 2012

Last Update Submit

August 1, 2018

Conditions

Obesity

Keywords

obesitysatietybody weight management

Outcome Measures

Primary Outcomes (1)

  • Correlation of subjective and objective satiety responses

    Comparison of subjective responses and gut hormone responses of satiety

    measures at -30, -15, 0, 15, 30, 60, 90, 120, 150, 180, 210, 240, 300 minutes

Secondary Outcomes (1)

  • Repeatability of subjective and objective measures of satiety

    measures at -30, -15, 0, 15, 30, 60, 90, 120, 150, 180, 210, 240, 300 minutes

Eligibility Criteria

Age25 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Healthy men and women

You may qualify if:

  • medical history (interview) demonstrating good health
  • non-smoking
  • not taking steroid-based medications
  • not planning to or currently attempting to gain or lose weight
  • being willing to consent to study conditions
  • healthy adults ages 25-45 years
  • body mass index between 18-30 kg/m2.
  • University of North Dakota students may participate but student status is not required.

You may not qualify if:

  • diagnosed eating disorders
  • current or planned pregnancy
  • lactation
  • unmanaged hypertension (systolic \>160 mmHg or diastolic \> 100mmHg) and/or other cardiovascular, pulmonary, skeletal and metabolic diseases
  • taking medications known to affect appetite, body composition, weight, or food intake

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

USDA Human Nutrition Research Center

Grand Forks, North Dakota, 58203, United States

Location

Biospecimen

Retention: SAMPLES WITHOUT DNA

blood samples

MeSH Terms

Conditions

Obesity

Condition Hierarchy (Ancestors)

OverweightOvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Susan K Raatz, PhD

    USDA GFHNRC

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
FED
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 3, 2012

First Posted

January 9, 2012

Study Start

July 1, 2012

Primary Completion

August 1, 2014

Study Completion

August 1, 2014

Last Updated

August 3, 2018

Record last verified: 2018-08

Data Sharing

IPD Sharing
Will not share

Locations

US(1)