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Electronic Health Record Strategies to Promote Diverse Participation in Research AIM 2

Yale University logo

Yale University

Status

Completed

Conditions

Patient Participation

Treatments

Other: Direct to Patient Message - Optimized
Other: Optimized Letter
Other: Traditional Letter
Other: Direct to Patient Message

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT06467487
2000032716_a
75F40120C00174 (Other Grant/Funding Number)

Details and patient eligibility

About

Based on the outcomes of the initial study (NCT05348603), this optimization study will employ the most effective interventions (letters and messages) and distribute these communications to underrepresented minorities to further promote interest in research. Optimized language will be distributed in English, Spanish, Portuguese, Chinese, Arabic, or Haitian Creole, based on preferred language identified in the patient profile in an electronic medical records system.

Full description

The primary objective of the optimization study is to examine the effectiveness on increasing interest in research of an optimized letter versus a generic letter; an optimized message versus a generic message; and an optimized letter and an optimized message versus a generic letter and a generic message.

The secondary objective of the optimization study is to examine the effectiveness on increasing participation in research of an optimized letter versus a generic letter, an optimized message versus a generic message, an optimized letter and an optimized message versus a generic letter and a generic message.

Enrollment

214,526 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Has an account with the online patient portal
  • Has logged into the online patient portal at least once in the past year
  • Has not set up a research profile

Exclusion criteria

  • Currently enrolled in a clinical trial
  • Opted out of research
  • On active cancer treatment
  • Active member of the study team

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

214,526 participants in 6 patient groups

Optimized Letter
Experimental group
Description:
Participants receive an 'optimized' letter.
Treatment:
Other: Optimized Letter
Optimized Message
Experimental group
Description:
Participants receive an 'optimized' message.
Treatment:
Other: Direct to Patient Message - Optimized
Optimized Letter + Optimized Message
Experimental group
Description:
Participants receive both a 'optimized' letter and a 'optimized' message.
Treatment:
Other: Direct to Patient Message - Optimized
Other: Optimized Letter
Generic Letter
Active Comparator group
Description:
Participants receive a 'usual' letter.
Treatment:
Other: Traditional Letter
Generic Message
Active Comparator group
Description:
Participants receive a 'usual' message.
Treatment:
Other: Direct to Patient Message
Generic Letter + Generic Message
Experimental group
Description:
Participants receive both a 'usual' letter and a 'usual' message.
Treatment:
Other: Direct to Patient Message
Other: Traditional Letter

Trial contacts and locations

1

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Central trial contact

Helen Seow, PhD

Data sourced from clinicaltrials.gov

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