Health TrialsbyHealthPanel

Evaluation of Report-Back Strategies for Long-term and Short-term Exposure Information in Rural Tribal Populations

ConditionBehavior Change
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Utah

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Enrolled member of the participating tribe

Disqualifiers

Participant in one of our previous studies

Trial design

Design model

Parallel

Treatments tested in this trial

  • Messenger 1

    Behavioral

    The first type of messenger (specific details TBD) that will be used to deliver the environmental sampling results.

  • Messenger 2

    Behavioral

    The second type of messenger (specific details TBD) that will be used to deliver the environmental sampling results.

  • Format 1

    Behavioral

    The first type of format (specific details TBD) that will be used to deliver the environmental sampling results.

  • Format 2

    Behavioral

    The second type of format (specific details TBD) that will be used to deliver the environmental sampling results.

Treatment groups

112 Participants
are divided into 2 treatment groups
Group A: Real-Time Exposure DataExperimental treatment 4 interventions
Group B: Delayed Exposure DataExperimental treatment 4 interventions

Trial outcomes

Primary outcomes

1

Exposure Reduction Behaviors

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.

Time frame
3 months after report-back
2

Exposure Reduction Behaviors

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.

Time frame
6 months after report-back
3

Exposure Reduction Behaviors

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.

Time frame
12 months after report-back

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Utah

Lead sponsor

National Institute of Environmental Health Sciences (NIEHS)

Collaborator

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: