NCT01888913

Brief Summary

Background: \- We are studying people s psychological experiences and how these relate to the way people respond have when they see information communicated in different ways. We are testing multiple research questions in this research. Objectives: \- To learn about how to design future research studies. Also to learn about how to best give people information about health topics. Eligibility: \- Women with a Body Mass Index of 25 or higher. Design:

  • Before the study visit, participants will answer some questions online about themselves, their experiences, and their thoughts about their weight.
  • During the study visit, participants will watch a short scene from a movie, and then answer questions about it.
  • Participants will have a simulated doctor visit with a computerized, virtual reality doctor. They will answer more questions about themselves, their experiences, and their thoughts about their weight. Then they will answer questions with researchers.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
1,464

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2013

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

June 26, 2013

Completed
2 days until next milestone

First Posted

Study publicly available on registry

June 28, 2013

Completed
7 days until next milestone

Study Start

First participant enrolled

July 5, 2013

Completed
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 10, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 10, 2016

Completed
Last Updated

June 20, 2024

Status Verified

June 1, 2024

Enrollment Period

2.6 years

First QC Date

June 26, 2013

Last Update Submit

June 18, 2024

Conditions

Keywords

Body WeightVirtual EnvironmentNatural History

Outcome Measures

Primary Outcomes (1)

  • A

    The primary goal of this research project is to continue building an evidence base on the benefits or pitfalls of introducing genomic information into weight-related primary care encounters.

    ongoing

Study Arms (1)

Adult Women

Adult Women aged 18-50

Eligibility Criteria

Age18 Years - 50 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

All participants will be adult women. Inclusion for Study 1 are: (1) being part of a Knowledge Networks Panel; (2) having a self-reported body mass index of greater than or equal to 25. Inclusion criteria for Study 2 are: (1) being between 18 and 50 years old; (2) having a self-reported body mass index of greater than or equal to 25; (3) having the ability to read, write, and converse in English; (4) being able to come to the NIH Clinical Center for one visit.

You may qualify if:

  • being between 18 and 50 years old;
  • having a self reported body mass index of greater than or equal to 25;
  • having the ability to read, write, and converse in English;
  • being able to come to the NIH Clinical Center for one visit.

You may not qualify if:

  • having a vestibular or seizure disorder;
  • having a high propensity for motion sickness;
  • known pregnancy;
  • uncorrected low vision or hearing;
  • inability to complete tasks in the virtual environment;
  • being or training to become a physician;

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Institutes of Health Clinical Center

Bethesda, Maryland, 20892, United States

Location

Related Publications (5)

  • Tetlock PE, Kristel OV, Elson SB, Green MC, Lerner JS. The psychology of the unthinkable: taboo trade-offs, forbidden base rates, and heretical counterfactuals. J Pers Soc Psychol. 2000 May;78(5):853-70. doi: 10.1037//0022-3514.78.5.853.

    PMID: 10821194BACKGROUND
  • Agurs-Collins T, Khoury MJ, Simon-Morton D, Olster DH, Harris JR, Milner JA. Public health genomics: translating obesity genomics research into population health benefits. Obesity (Silver Spring). 2008 Dec;16 Suppl 3(Suppl 3):S85-94. doi: 10.1038/oby.2008.517.

    PMID: 19037221BACKGROUND
  • Kushner RF. Understanding obesity by asking the right questions. Perspect Biol Med. 2010 Winter;53(1):148-51. doi: 10.1353/pbm.0.0139.

    PMID: 20201162BACKGROUND
  • Persky S, Ferrer RA, Klein WM. Nonverbal and paraverbal behavior in (simulated) medical visits related to genomics and weight: a role for emotion and race. J Behav Med. 2016 Oct;39(5):804-14. doi: 10.1007/s10865-016-9747-5. Epub 2016 May 4.

  • Persky S, Ferrer RA, Klein WM. Genomic Information may Inhibit Weight-Related Behavior Change Inclinations Among Individuals in a Fear State. Ann Behav Med. 2016 Jun;50(3):452-9. doi: 10.1007/s12160-016-9771-2.

Related Links

MeSH Terms

Conditions

Body Weight

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Susan Persky, Ph.D.

    National Human Genome Research Institute (NHGRI)

    PRINCIPAL INVESTIGATOR

Study Design

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

Study Record Dates

First Submitted

June 26, 2013

First Posted

June 28, 2013

Study Start

July 5, 2013

Primary Completion

February 10, 2016

Study Completion

February 10, 2016

Last Updated

June 20, 2024

Record last verified: 2024-06

Locations