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Communication Issues in Patient and Provider Discussions of Immunotherapy

Communication Issues in Patient/Provider Discussions of Immunotherapy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05873608
Enrollment
125
Registered
2023-05-24
Start date
2016-10-06
Completion date
2027-11-17
Last updated
2026-04-06

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

Conditions

Hematopoietic and Lymphoid System Neoplasm, Malignant Solid Neoplasm

Brief summary

This trials studies communication issues in patient and provider discussions about immunotherapy. The goal of this study is to describe where patients have heard about immunotherapy, what the participants understand about it, how physicians and other healthcare workers describe immunotherapy, and how educational videos may support patient knowledge about immunotherapy.

Detailed description

PRIMARY OBJECTIVES: I. To identify misestimations about the risks and benefits of immunotherapy resulting from media hype or other sources and assess if these misestimations persist post-provider conversation about immunotherapy. II. To qualitatively describe patient reported misunderstandings and to assess patient understanding of technical terms and metaphors used in the immunotherapy conversation. III. To identify provider and patient preferences for information to be communicated about immunotherapy. IV. Develop videos that describe immunotherapy and test their efficacy in improving understanding using pre and post methodology. OUTLINE: Patients and their providers undergo observation during a conversation about immunotherapy. Then participate in an interview over 20 minutes. Understanding of educational videos is then tested.

Interventions

OTHEREducational video

Testing an educational video

OTHERInterview

Participate in interview

OTHERObservation

Undergo observation

Sponsors

Emory University
Lead SponsorOTHER
National Cancer Institute (NCI)
CollaboratorNIH

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

For aim 4, each participant is assigned to watch a video and comprehension is tested using a pre and post method

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* AIMS 1-3: All patients and providers who may have a discussion about immunotherapy at the Winship Cancer Institute * AIM 4: Any cancer patient

Design outcomes

Primary

MeasureTime frameDescription
Misestimations about the risks and benefits of immunotherapy resulting from media hype or other sourcesUp to 4 yearsWill use descriptive statistics to summarize the demographic characteristics and responses to the interviews. Will audio-record and transcribe the provider conversation for immunotherapy and the pre- and post-provider conversation interviews. The transcripts will be qualitatively coded using multi-level semantic analysis in MAXQDA. Pre-determined codes will include a list of potential benefits of immunotherapy, any patient estimation of the potential for benefit, any side effect and risk mentioned and any estimation of its frequency. Because there is no data on the frequency of misestimations due to media hype, no quantitative analysis is planned.
Qualitatively describe patient reported misunderstandingsUp to 4 yearsDuring the observed conversation, the ethics team member will note any technical term or metaphor used. The patient will then be asked if each term and metaphor is understood. The open ended questions about misunderstanding, technical terms and metaphors used, and patients' understanding of each term will be qualitatively coded using multi-level semantic analysis in MAXQDA. Frequency of misunderstood terms and misunderstood metaphors will be calculated.
Provider and patient preferences for information to be communicated about immunotherapyUp to 4 yearsThe frequencies of each item of information identified by providers and patients will be determined. A combined list of the most frequently mentioned items of information to be included and a discussion of immunotherapy will be compiled.
Correct definition rates (pre- versus post-video)Up to 4 yearsBefore-video and after-video correct definition rates will be calculated, along with 95% exact binomial confidence intervals using the Clopper-Pearson method. Before and after paired rates will be compared using an exact McNemar's test. Subset analyses will be performed for gender, age group (=\< 55, \> 55), and education level (high school graduate or less, some college or more).

Countries

United States

Contacts

CONTACTRebecca Pentz, PhD
rpentz@emory.edu404-778-5694
PRINCIPAL_INVESTIGATORRebecca Pentz, PhD

Emory University Hospital/Winship Cancer Institute

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 7, 2026