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Impacts of a Report-back Training Program

Expanding Effective Report-back of Environmental Exposures Among New Researchers

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06046872
Enrollment
56
Registered
2023-09-21
Start date
2023-06-22
Completion date
2024-12-15
Last updated
2026-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Behavioral Shift (Researcher Willingness to Report-back)

Brief summary

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.

Detailed 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.

Interventions

BEHAVIORALReport-back training

Researchers participate in a report-back training program to evaluate potential impacts on knowledge and future behaviors with respect to sharing personal exposure results with study participants.

Sponsors

Silent Spring Institute
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

* Under 18

Design outcomes

Primary

MeasureTime frameDescription
Concern About Report-back, Before and After Training ProgramParticipants completed surveys before and after the single-day training program.Participants ranked how strongly they agreed with each of 3 statements about concerns about report-back using a Likert-scale from 1 (strongly disagree) to 5 (strongly agree). Responses were summed together to calculate sum concern (3-15). Higher values indicate greater concern about report-back so a higher post-test score would indicate a worse outcome (i.e., that concern about report-back increased as a result of the training program.
Perceived Benefits of Report-back, Before and After Training ProgramParticipants completed surveys before and after the single-day training program.Participants ranked how strongly they agreed with each of 5 statements about perceived benefits of report-back using a Likert-scale from 1 (strongly disagree) to 5 (strongly agree). Responses were summed together to calculate sum perceived benefits (5-25). Higher values indicate stronger agreement with perceived benefits, so a higher post-test score would indicate a better outcome (i.e., that perceived benefits of report-back increased as a result of the training program).
Beliefs About Report-back, Before and After Training ProgramParticipants completed surveys before and after the training program.Participants ranked how strongly they agreed with each statement using a Likert-scale from 1 (strongly disagree) to 5 (strongly agree).

Countries

United States

Participant flow

Recruitment details

We facilitated report-back training workshops, including two in-person workshops at the International Society for Epidemiology (ISEE) and Partnerships for Environmental Public Health (PEPH) conferences, and three virtual workshops. Participants were recruited through conferences advertising the workshops (e.g., during conference registration), and through emailing individuals directly from a list we compiled of NIH-funded environmental health researchers.

Pre-assignment details

Participants were not assigned to an arm or group. Rather, for all individuals who participated in a report-back training program, we evaluated any shifts in participants perspectives on environmental health report-back and wiliness to report-back with pre- and post-tests.

Baseline characteristics

Characteristic
Ethnicity (NIH/OMB)
Hispanic or Latino
7 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
26 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
23 Participants
Race (NIH/OMB)
American Indian or Alaska Native
1 Participants
Race (NIH/OMB)
Asian
2 Participants
Race (NIH/OMB)
Black or African American
0 Participants
Race (NIH/OMB)
More than one race
2 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
25 Participants
Race (NIH/OMB)
White
26 Participants
Region of Enrollment
United States
56 Participants
Sex/Gender, Customized
Female
29 Participants
Sex/Gender, Customized
Male
4 Participants
Sex/Gender, Customized
Sex/gender unknown
23 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 0
other
Total, other adverse events
0 / 0
serious
Total, serious adverse events
0 / 0

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 8, 2026