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NCT Number: NCT07656584

Implementation of Communication Disability Collection and Accommodations in Primary Care Settings

This multi-methods-multi-site study aims to adapt and evaluate the effects of an implementation support package of strategies to assist primary care clinics in documenting patients' communication disability (CD) and accommodation needs in the electronic health record (EHR) and providing communication accommodations through EHR data extraction, surveys, focus groups, interviews, and clinical practice observations.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

EHR Data Extraction

  • Adults 18+ years
  • Patients who had at least one visit within the 21-month EHR data collection period at participating study clinics.

Clinic Leadership, Providers & Clinic Staff

  • Adults 18+ years
  • Individuals of all genders and members of all racial and ethnic categories employed at participating study clinics will be eligible for inclusion. NYULH study personnel will enroll providers and staff referred for study inclusion from all participating study clinics; not just NYULH staff exclusively.

Patients

  • Adults 18+ years
  • Patients with communication disabilities seen at least once at participating study clinics during the 21-month study period.
  • Patients who self-identify as proficient in English communication as defined by English being a preferred language, or self-reported ability to participate in an interview in English without the support of an interpreter.

Exclusion criteria

EHR Data Extraction

  • Patients whose records are unavailable due to technical issues.
  • Patients who are not seen at least once at participating study clinics during the 21-month data collection period.
  • Duplicate records (e.g., duplicative EHR records marked for deletion).
  • Patients who have opted-out of research participation.

Clinic Leadership, Providers & Clinic Staff Interviews and Focus Groups

  • Being <18 years old
  • Not an employed member of a participating study clinic or potential end user of the study implementation strategy.

Patient Interviews

  • Being <18 years old
  • Patients without communication disabilities.
  • Patients with communication disabilities seen outside of participating study clinics.
  • Patients who are unable to provide consent for themselves.
  • Patients who report not being proficient in English communication or self-reported inability to participate in an interview in English without the support of an interpreter.

Treatment and study plan

Implementation Support Package

Behavioral

The implementation support package includes materials, activities, and procedures ready for use in diverse primary care practices and will facilitate each clinic's determination of how they will implement collection of disability status and provision of accommodations.

Primary outcomes

  1. (Aim 2) Patient Reach

    Time frame: Baseline, Implementation Follow Up (Approximately Month 9), Maintenance Follow Up (Approximately Month 21)

    Percent of patients who have a visit during the time of data collection and have the communication disability field completed in the EHR. A positive outcome for having the communication disability field completed in the EHR will be "no disability" "speech/language disability", "hearing disability", "decline", or "other" documented in the EHR, while a negative outcome will be the CD fields being left blank. All adult patients who are seen in each clinic are eligible to have their disability status documented, regardless of the type of visit.

  2. (Aim 3) Adoption

    Time frame: Implementation Follow Up (Approximately Month 9), Maintenance Follow Up (Approximately Month 21)

    Adoption assessed for all the patients with a recorded accommodation need; measured as the percentage of clinical encounters in which the accommodation was provided and used, as ascertained through the EHR.

Study contacts

Contact information is provided by the study sponsor or research team.

Megan Morris, PhD

CONTACT

[email protected]

646-501-0027

Sankeerth Jinna

CONTACT

[email protected]

2122630844

Sponsors and collaborators

Lead sponsor

NYU Langone Health

Other

Registry information

Acronym: DECA

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jun 18, 2026
Registry last updated
Jul 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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