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Clinical Trials/NCT05268055
NCT05268055CompletedNot Applicable

Sign Here: How to Conduct Informed Consent With Deaf Individuals

University of Massachusetts, Worcester2 sites in 1 country208 target enrollmentStarted: May 3, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
208
Locations
2
Primary Endpoint
Healthcare Provider Cultural Competency

Study Overview

Brief Summary

The goal of this research is to create a training film for hearing healthcare providers to teach them how to competently and sensitively interact with Deaf patients. In Year 1, focus groups will be facilitated to elicit feedback that will inform video production of the training film. In Year 2, film production will take place, as well as a randomized clinical trial (RCT) to test the feasibility and preliminary efficacy of the new training intervention.

Detailed Description

The U.S. Deaf community - a minority group of more than 500,000 people who use American Sign Language (ASL) - is one of the most understudied and underserved populations within our nation's healthcare system. Reasons for this underrepresentation include lack of language access in healthcare and research settings, as well as communal feelings of mistrust toward the medical community. For example, healthcare providers and clinical researchers follow a medical model to "cure" or "fix" deafness, whereas most Deaf people do not want to be fixed, but rather to be respected as a cultural and linguistic minority group.

To begin to rectify this mistrust and underrepresentation, the informed consent process has been suggested as a key area of intervention. From 2016 - 2018, our team produced a film to train research personnel to effectively interact with Deaf research participants during the informed consent process. The intervention was designed through a two-year collaboration with the local Deaf community - community forums, focus groups, and an intervention development team inclusive of Deaf researchers, filmmakers, and laypeople.

In 2022, our team conducted a second series of focus groups with key stakeholders to refine, expand, and tailor a new version of the Sign Here training film for healthcare providers. Filmmaking is currently underway. In April 2023, we will launch a randomized controlled trial to test the feasibility, acceptability, and preliminary efficacy of the new training intervention. Eighty healthcare providers, medical students, and nursing students will be randomized to receive (1) the Sign Here training film or (2) an "intervention as usual" condition (i.e., standard written guidance on how to communicate with Deaf patients in healthcare settings). Primary outcomes are provider cultural competence, communication skill, and ability to build trust, which will be tested via virtual simulation with a Deaf standardized patient.

Results will potentially validate a product of immediate value - a highly-accessible, easy-to-disseminate training film to promote the inclusion of Deaf people in our nation's healthcare system. Results will also inform the design of a large, multi-institution study to explore the real-world scalability of the Sign Here training film in medical schools across the U.S.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • self-identification as a healthcare provider, medical student, or nursing student
  • current or recent engagement in informed consent for treatment
  • access to an informed consent form that can be used for a simulated informed consent session
  • We will also screen participants' self-reported level of experience with Deaf people, as we aim to recruit participants with little-to-no prior experience interacting with Deaf people to reflect the most probable real-word encounter that a Deaf person would have when receiving healthcare services.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Healthcare Provider Cultural Competency

Time Frame: post-intervention, up to one month

A validated scale used to measure provider cultural competence. Total scores range from 9 to 63, with higher scores indicative of higher levels of cultural competency.

Ask, Understand, Remember Assessment

Time Frame: post-intervention, up to one month

A validated scale used to measure participants' communication skill. Total scores range from 4 to 16, with higher scores indicating better communication skills.

Wake Forest Physician Trust Scale

Time Frame: post-intervention, up to one month

A validated scale used to measure the ability to build trust with the standardized patient/participant. Total scores range from 10 to 50, with higher scores indicating greater ability to build trust.

Secondary Outcomes

  • Assessment of Intervention Understanding & Retention(post-intervention, up to one month)
  • Self-Rating of Simulation(post-intervention, up to one month)

Investigators

Sponsor
University of Massachusetts, Worcester
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Melissa L. Anderson

Associate Professor of Psychiatry

University of Massachusetts, Worcester

Study Sites (2)

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