- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06593340
Evaluation of Report-Back Strategies for Long-term and Short-term Exposure Information in Rural Tribal Populations
The goal of this study is to evaluate different ways to provide feedback about environmental sampling results to participants. Specifically, the study will look at exposures with long-term risk (radon) and short-term risk (indoor particulate matter, PM2.5). The hypothesis is that providing feedback in real-time will result in participants engaging in more activities to try to reduce their exposure. One of the main questions of interest is: How does the information messenger impact the effectiveness of report-back strategies in rural, tribal populations?
Participants will have radon and PM2.5 measurement equipment installed at their home and will answer questions about any actions they took to reduce exposure. Previously developed approaches to reporting back those exposures will be used to test which feedback method results in more actions to reduce exposure.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Darrah K Sleeth, PhD
- Phone Number: 801-585-3587
- Email: darrah.sleeth@hsc.utah.edu
Study Contact Backup
- Name: Scott Collingwood, PhD
- Phone Number: 801-213-3726
- Email: scott.collingwood@hsc.utah.edu
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Enrolled member of the participating tribe
Exclusion Criteria:
- Participant in one of our previous studies
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Real-Time Exposure Data
Participants in this arm will get their data reported-back in real-time.
There will be a total of 4 different strategies tested based on a combination of two (2) messengers and two (2) formats tested.
|
The first type of messenger (specific details TBD) that will be used to deliver the environmental sampling results.
The second type of messenger (specific details TBD) that will be used to deliver the environmental sampling results.
The first type of format (specific details TBD) that will be used to deliver the environmental sampling results.
The second type of format (specific details TBD) that will be used to deliver the environmental sampling results.
|
|
Experimental: Delayed Exposure Data
Participants in this arm will get their data reported-back only after all exposure data are collected (i.e., delayed approximately 2 months).
There will be a total of 4 different strategies tested based on a combination of two (2) messengers and two (2) formats tested.
|
The first type of messenger (specific details TBD) that will be used to deliver the environmental sampling results.
The second type of messenger (specific details TBD) that will be used to deliver the environmental sampling results.
The first type of format (specific details TBD) that will be used to deliver the environmental sampling results.
The second type of format (specific details TBD) that will be used to deliver the environmental sampling results.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Exposure Reduction Behaviors
Time Frame: 3 months after report-back
|
This will be collected using a questionnaire with a likert scale from 1 (not at all) to 10 (a lot) of how often certain exposure-reduction behaviors are performed.
|
3 months after report-back
|
|
Exposure Reduction Behaviors
Time Frame: 6 months after report-back
|
This will be collected using a questionnaire with a likert scale from 1 (not at all) to 10 (a lot) of how often certain exposure-reduction behaviors are performed.
|
6 months after report-back
|
|
Exposure Reduction Behaviors
Time Frame: 12 months after report-back
|
This will be collected using a questionnaire with a likert scale from 1 (not at all) to 10 (a lot) of how often certain exposure-reduction behaviors are performed.
|
12 months after report-back
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01ES036260 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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