NCT02874053

Brief Summary

Background: People with cancer often have to make complex decisions about their treatment. For some of these decisions, they have to weigh the benefits of a treatment against its side effects. They may have to think about its potential to increase the risk of another disease. One example is hormone replacement therapy. That reduces a woman s risk of getting colorectal cancer, but it raises her risk of getting breast cancer. Researchers want to learn more about how people make tradeoff decisions like these. Objective: To learn about how people respond to information about hypothetical health and medical treatment options. Eligibility: Adults ages 18 70. Design: Participants will have one 30-minute visit. Participants will complete a series of short questionnaires. These will be about their beliefs and values. Some may be about cancer and heart disease risk. Participants ages 18 to 29 will answer questions about sexual health. Participants will write a paragraph or two about a room in their house or about a life event. Participants will read a series of stories. These will describe different hypothetical health treatments. The stories describe a pill that lowers the risk of one health condition, but raises the risk for another. After each story, participants will note how willing they are to take the pill. Participants will answer questions about the information that they got. They will also answer questions about their health, beliefs, and opinions. Participants will do 2 attention tasks computer.

Trial Health

15
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Timeline
Completed

Started Jun 2019

Status
withdrawn

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 17, 2016

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 22, 2016

Completed
2.8 years until next milestone

Study Start

First participant enrolled

June 5, 2019

Completed
12 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 17, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 17, 2019

Completed
Last Updated

June 19, 2019

Status Verified

June 1, 2019

Enrollment Period

12 days

First QC Date

August 17, 2016

Last Update Submit

June 18, 2019

Conditions

Keywords

Risk PerceptionsMedical TradeoffsRegulatory FocusIntegral Affect

Outcome Measures

Primary Outcomes (1)

  • willingness to take hypothetical pill

    self-reported behavioral willingness

    at baseline (cross-sectional)

Study Arms (1)

Healthy

Healthy Volunteers

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Community members and students from the University of Pittsburgh.

You may qualify if:

  • For Study A, community members will be invited to participate if they are aged 18 to 70.
  • For Study B, University at Pittsburgh students will be invited to participate if they are aged 18 and over.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (2)

  • Lockwood P, Jordan CH, Kunda Z. Motivation by positive or negative role models: regulatory focus determines who will best inspire us. J Pers Soc Psychol. 2002 Oct;83(4):854-64.

    PMID: 12374440BACKGROUND
  • Waters EA, Weinstein ND, Colditz GA, Emmons KM. Aversion to side effects in preventive medical treatment decisions. Br J Health Psychol. 2007 Sep;12(Pt 3):383-401. doi: 10.1348/135910706X115209.

    PMID: 17640453BACKGROUND

MeSH Terms

Conditions

Neoplasms

Study Officials

  • William M Klein

    National Cancer Institute (NCI)

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
NIH
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 17, 2016

First Posted

August 22, 2016

Study Start

June 5, 2019

Primary Completion

June 17, 2019

Study Completion

June 17, 2019

Last Updated

June 19, 2019

Record last verified: 2019-06