NCT02267928

Brief Summary

Prevention and early detection of medical problems can greatly reduce health care costs, yet time and again, people avoid or ignore services that could help detect medical problems early enough to prevent or reduce the severity of potential problems. The investigators seek to understand whether the elicitation of symptom admission by patients can predict people's perceived risk of the medical condition and voluntary pursuit of medical information.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
305

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2014

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

Study Start

First participant enrolled

October 1, 2014

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

October 14, 2014

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 20, 2014

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2016

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2016

Completed
Last Updated

August 2, 2016

Status Verified

August 1, 2016

Enrollment Period

1.4 years

First QC Date

October 14, 2014

Last Update Submit

August 1, 2016

Conditions

Keywords

Symptom Assessment

Outcome Measures

Primary Outcomes (3)

  • Number of symptoms

    The number of symptoms checked off by participants

    1 day

  • Risk of meningioma

    Self-reported perceived risk of meningioma

    1 day

  • Information pursuit

    Binary measure of whether participants click to receive information about meningioma

    1 day

Secondary Outcomes (2)

  • Funding allocation

    1 day

  • Risk of serious disease

    1 day

Study Arms (4)

Check/Experience

EXPERIMENTAL

Participants are asked to check the symptoms that they have experienced in the last 6 weeks.

Other: Check SymptomsOther: Experienced

Un-check/Experience

EXPERIMENTAL

Participants are asked to un-check the symptoms that they have experienced in the last 6 weeks.

Other: Uncheck SymptomsOther: Experienced

Check/Not Experienced

EXPERIMENTAL

Participants are asked to check the symptoms that they have NOT experienced in the last 6 weeks.

Other: Check SymptomsOther: Not Experienced

Un-check/Not Experienced

EXPERIMENTAL

Participants are asked to un-check the symptoms that they have NOT experienced in the last 6 weeks.

Other: Uncheck SymptomsOther: Not Experienced

Interventions

Symptoms are "Checked"

Check/ExperienceCheck/Not Experienced

Symptoms are "Un-checked"

Un-check/ExperienceUn-check/Not Experienced

Focus of instructions is on symptoms the participant has experienced

Check/ExperienceUn-check/Experience

Focus of instructions is on symptoms the participant has NOT experienced

Check/Not ExperiencedUn-check/Not Experienced

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • or older
  • American

You may not qualify if:

  • Mechanical Turk approval rate below 95%

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Carnegie Mellon University

Pittsburgh, Pennsylvania, 15213, United States

Location

MeSH Terms

Conditions

Meningioma

Interventions

Coping Orientation to Problems Experienced Questionnaire

Condition Hierarchy (Ancestors)

Neoplasms, Nerve TissueNeoplasms by Histologic TypeNeoplasmsNeoplasms, Vascular TissueMeningeal NeoplasmsCentral Nervous System NeoplasmsNervous System NeoplasmsNeoplasms by SiteNervous System Diseases

Study Officials

  • Eric M VanEpps, MS

    Carnegie Mellon University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SCREENING
Intervention Model
FACTORIAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD Candidate

Study Record Dates

First Submitted

October 14, 2014

First Posted

October 20, 2014

Study Start

October 1, 2014

Primary Completion

March 1, 2016

Study Completion

May 1, 2016

Last Updated

August 2, 2016

Record last verified: 2016-08

Locations