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NCT06919653 · ClinicalTrials.gov registry record · NA

Promoting Adherence to Chemotherapy Handling Guidelines Among Oncology Nurses

A NA study, sponsored by University of Cincinnati.

Not yet
Registry status
NA
Development phase
60
Enrollment target

NCT06919653: Clinical Trial NA study, sponsored by University of Cincinnati.

NCT06919653 is a NA study that has not yet begun recruiting, run by University of Cincinnati. The registered enrollment target is 60 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06919653, a NA study, has not yet begun recruiting, sponsored by University of Cincinnati.

NOT YET RECRUITING
Registry status
NA
Development phase
60 participants
Enrollment target

Study Summary

Chemotherapy exposure is a serious occupational hazard affecting oncology nurses. Oncology nurses' adherence to chemotherapy handling guidelines is essential to prevent their exposure to chemotherapy. The goal of this research is to develop, validate, and pilot test an intervention "Workplace program to Improve Safe Handling of hazardous drugs" (WISH), to promote adherence to chemotherapy handling guidelines among oncology nurses. The WISH intervention includes two components: an educational component and debriefing sessions on chemotherapy exposure incidents. First, the research team will use a mixed-methods approach to develop an online educational component on chemotherapy safety, establish the content validity of the educational content based on experts' evaluation, and establish the face validity of the educational content by conducting three qualitative focus group with oncology nurses (n=4-6 nurses per group) or individual interviews. Next, the research team will test the feasibility and acceptability of the intervention using a pilot randomized controlled trial with two groups of oncology nurses, an intervention group (n= 30) and a control group (n=30). We will obtain quantitative and qualitative measures of the intervention feasibility and acceptability. The output is an intervention program targeted to train nurses on safe chemotherapy handling guidelines. Findings will be disseminated through peer-reviewed publications and presentations. The intermediate outcome is the adoption of the intervention program by healthcare institutions to train nurses on chemotherapy handling guidelines. The end outcome is promoting adherence to chemotherapy handling guidelines among oncology nurses.

Primary Outcome

This variable will be measured using Hazardous Drug Handling Questionnaire. The scores reflect the percentage of time nurses adhere to chemotherapy handling guidelines and range between 0%-100%. A higher score indicates greater adherence to chemotherapy handling guidelines.

Interventions

  • BEHAVIORAL The Workplace program to Improve the Safe Handling of hazardous drugs (WISH)

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2026-06
Est. Completion 2027-08
Phase NA
University of Cincinnati

245 total trials

What is known before NCT06919653 opens enrollment

NCT06919653 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 1 intervention - of which The Workplace program to Improve the Safe Handling of hazardous drugs (WISH) is the first listed.

NCT06919653 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06919653 about?

NCT06919653 is a clinical study titled "Promoting Adherence to Chemotherapy Handling Guidelines Among Oncology Nurses". Chemotherapy exposure is a serious occupational hazard affecting oncology nurses. Oncology nurses' adherence to chemotherapy handling guidelines is essential to prevent their exposure to chemotherapy. The goal of this research is to develop, validate, and pilot test an intervention "Workplace progra...

What is the current status of trial NCT06919653?

This trial is currently not yet recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2026-06. Estimated completion is 2027-08.

What interventions are being tested in trial NCT06919653?

The interventions under investigation include: The Workplace program to Improve the Safe Handling of hazardous drugs (WISH) (BEHAVIORAL).

Who is sponsoring clinical trial NCT06919653?

This trial is sponsored by University of Cincinnati, which has 245 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06919653's enrollment target sits among peer trials

60 1164th of 2000 higher than 745 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06919653, the US trial registry maintained by the National Library of Medicine. NCT06919653 (small enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.