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TeamTalk: Improving Inter-professional Communication During Cancer Treatment

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The Washington University

Status

Begins enrollment in a year or more

Conditions

Pediatric Cancer

Treatments

Behavioral: Multi-level communication intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT07083674
1R01CA287374 (U.S. NIH Grant/Contract)
202503183

Details and patient eligibility

About

This study focuses on improving interprofessional communication during cancer treatment, through an individual and hospital system intervention, to improve provider outcomes, patient care, and, ultimately, survival for children with cancer in low-resource settings.

Enrollment

8 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hospitals identified as being in lowest quartile of communication quality, as defined by prior cross-sectional CritCom analysis and measured as the overall CritCom score.
  • All Global Alliance hospitals providing childhood cancer care will be eligible to participate.
  • Individual participants will be included if they care for hospitalized children with cancer at risk of deterioration.

Exclusion criteria

  • None

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

8 participants in 2 patient groups

Intervention Group
Experimental group
Description:
This study includes an intervention development phase (Aim 2) during which the intervention content and delivery mechanisms will be finalized. We will implement the multilevel intervention developed in Aim 2. We anticipate this will consist of one instance of intervention at each hospital and we will develop a full intervention manual following Aim 2. Details regarding the intervention will be updated prior to participant enrollment in the trial.
Treatment:
Behavioral: Multi-level communication intervention
Waitlist Control Group
No Intervention group
Description:
The wait list control is a group that does not receive an intervention during the study period, serving as an untreated comparison during the study, although they later receive the intervention. This intervention will be delivered after the completion of the last data collection instance.

Trial contacts and locations

1

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Central trial contact

Sara Malone, LCSW, PhD

Data sourced from clinicaltrials.gov

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