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Impacts of a Report-back Training Program

S

Silent Spring Institute

Status

Completed

Conditions

Behavioral Shift (Researcher Willingness to Report-back)

Treatments

Behavioral: Report-back training

Study type

Interventional

Funder types

Other

Identifiers

NCT06046872
1R21ES032934-01A1

Details and patient eligibility

About

Researchers participate in a hands-on training program on returning personal exposure results, and pre- and post-tests assess outcomes shifts in knowledge and perspectives on its value, and willingness to implement report-back in current or future studies.

Full description

The investigators study the outcomes from a program that trains researchers to implement report-back, informs perspectives on the value of report-back, increases likelihood of adoption, and promotes insights from visualization of results. The investigators evaluate the training using pre- and post-tests. The training program includes an introductory module on ethical and practical benefits and best practices for report-back. This is followed by a session where researchers gain hands-on practice in report preparation using Digital Exposure Report-Back Interface (DERBI), a digital report-back tool. Pre- and post-tests assess outcomes related to their prior concerns about report-back, knowledge about report-back, shifts in perspectives on its value, novel insights about data from Researcher- DERBI, and willingness to implement report-back in current and future studies.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Must be affiliated with a study that collects biomonitoring or personal exposure data

Exclusion criteria

  • Under 18

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 1 patient group

Report-back training program
Other group
Description:
Researchers participate in a training program on sharing personal results. Pre-and post-tests are administered to evaluate shifts in perspectives and wiliness to report-back before and after the training program. There is no control group.
Treatment:
Behavioral: Report-back training

Trial contacts and locations

1

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Central trial contact

Jennifer Ohayon, PhD

Data sourced from clinicaltrials.gov

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