← Back to Search

Report-back Training for Reporting Bias

N/A

Recruiting

Research Sponsored by Silent Spring Institute

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up 3 hours (the training is approximately three hours and pre-and post-tests are administered directly before and after)

Awards & highlights

Study Summary

This trial helps researchers learn how to share study results with participants and understand the importance and benefits of doing so.

Who is the study for?

This trial is for researchers involved in studies that collect biomonitoring or personal exposure data. Participants must be adults, meaning they are over the age of 18.Check my eligibility

What is being tested?

The trial tests a training program designed to teach researchers how to effectively communicate personal exposure results back to participants. It measures changes in knowledge, attitudes towards the value of report-back, and readiness to use these methods in their work.See study design

What are the potential side effects?

Since this study involves an educational training program rather than a medical intervention, traditional physical side effects are not applicable. However, there may be cognitive or emotional responses related to learning new information.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ 3 hours (the training is approximately three hours and pre-and post-tests are administered directly before and after)

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~3 hours (the training is approximately three hours and pre-and post-tests are administered directly before and after)

This trial's timeline: 3 weeks for screening, Varies for treatment, and 3 hours (the training is approximately three hours and pre-and post-tests are administered directly before and after) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Researcher wiliness to share personal exposure results as measured by pre- and post-tests administered alongside a training program

Trial Design

1Treatment groups

Experimental Treatment

Group I: Report-back training programExperimental Treatment1 Intervention

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.

Do I qualify?Apply below to find out

Find a Location

Who is running the clinical trial?

Silent Spring InstituteLead Sponsor

1 Previous Clinical Trials

400 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there any available slots for people to participate in this research?

"Data from clinicaltrials.gov affirms that this medical trial is presently recruiting participants. The posting of the study initially occurred on June 22nd 2023 and was most recently revised September 13th 2023."

Answered by AI

What is the current capacity of this clinical research endeavor?

"Yes, evidence from clinicaltrials.gov indicates that the trial is recruiting participants. It was initially posted on June 22nd 2023 and recently revised on September 13th 2023. Just 40 patients are needed for this single-site study."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

Impacts of a Report-back Training Program

Jennifer Ohayon 2023. "Impacts of a Report-back Training Program". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT06046872.