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Social Norms, Messengers, and Processing Fluency to Increase Hypertension Medication Adherence

Mass General Brigham logo

Mass General Brigham

Status

Completed

Conditions

Hypertension
Medication Adherence

Treatments

Behavioral: Processing fluency
Behavioral: Messenger effects
Behavioral: Social norms
Behavioral: Scorecard

Study type

Interventional

Funder types

Other
Industry
NIH

Identifiers

NCT06066541
P30AG064199 (U.S. NIH Grant/Contract)
2023p002222

Details and patient eligibility

About

Medicare Advantage beneficiaries ages 65-79 and insured by Humana with at least two unique fills of hypertension medication within the 2023 calendar year and adherence level between 60 and 85% will be identified using Humana Medicare Advantage claims data. Individuals meeting these inclusion criteria will be included and, with an institutional review board approved waiver of informed consent, will be randomized to one of 6 mailed messages or control (no message). The messages will be sent by Humana and use different behavioral techniques (social norms, messenger effects, and/or processing fluency) providing their medication refill score. Humana will send a second message within 60 days of the first message noting any changes in the refill score.

The primary outcome will be the average end-of-year adherence in each arm. A secondary outcome will be the proportion of study participants with end-of-year adherence greater than or equal to 80%. The study team's hypothesis is that messages using dynamic social norms, messenger effects, and processing fluency in combination will more effectively increase average end-of-year adherence level compared to usual care.

Humana will conduct all study participant outreach and data analyses, which will be performed using routinely collected insurance claims data. Regulatory oversight is conducted using Humana's centralized institutional review board (IRB) of record. The work completed by Humana study staff is funded by Humana, Inc.

Dr. Choudhry and his colleagues (including subaward recipients ideas42 and Tuck School of Business at Dartmouth) will provide technical and subject matter expertise related to study research design and implementation, protocol design, statistical analysis, publication (abstract, poster, manuscript) preparation and/or review, and assistance throughout the peer review process including revisions and additional analyses if necessary for this project. The work completed by study staff at Brigham and Women's Hospital, ideas42, and Tuck School of Business at Dartmouth is funded by NIA.

Enrollment

65,177 patients

Sex

All

Ages

65 to 79 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Medicare Advantage beneficiary insured by Humana
  • Between the ages of 65 and 79
  • Having at least two unique fills of any class of hypertension medication within the calendar year (2023).
  • Adherence level (as measured by the proportion of days covered [PDC] metric) between 60% and 85%

Exclusion criteria

  • Beneficiaries in plans which, per contractual agreements, privacy policies and rules, or legal requirements, do not participate in research

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

65,177 participants in 7 patient groups

Scorecard
Active Comparator group
Description:
Participants randomized to this arm will receive a scorecard from Humana reporting patients' medication adherence using a "refill score." Two messages will be sent during the intervention: The first message will contain the baseline refill score. The second message will note any changes in the refill score.
Treatment:
Behavioral: Scorecard
Scorecard + Social norms
Experimental group
Description:
Participants randomized to this arm will receive the Arm 1 scorecard plus dynamic social norms messaging (noting the proportion of Humana members improving their medication refill scores). Two messages will be sent during the intervention: The first message will contain the baseline refill score. The second message will note any changes in the refill score.
Treatment:
Behavioral: Scorecard
Behavioral: Social norms
Scorecard + Messenger effects
Experimental group
Description:
Participants randomized to this arm will receive the Arm 1 scorecard, coming from the trusted messenger of a Humana-identified pharmacist taking the same medication. Two messages will be sent during the intervention: The first message will contain the baseline refill score. The second message will note any changes in the refill score.
Treatment:
Behavioral: Scorecard
Behavioral: Messenger effects
Processing fluency
Experimental group
Description:
Participants randomized to this arm will receive a modified scorecard increasing processing fluency through a visual metaphor of "closing the ring." Two messages will be sent during the intervention: The first message will contain the baseline refill score. The second message will note any changes in the refill score.
Treatment:
Behavioral: Processing fluency
Processing fluency + Social norms
Experimental group
Description:
Participants randomized to this arm will receive the Arm 4 processing fluency scorecard plus dynamic social norms messaging. Two messages will be sent during the intervention: The first message will contain the baseline refill score. The second message will note any changes in the refill score.
Treatment:
Behavioral: Social norms
Behavioral: Processing fluency
Processing fluency + Messenger effects
Experimental group
Description:
Participants randomized to this arm will receive the Arm 4 processing fluency scorecard coming from the trusted messenger of a Humana-identified pharmacist taking the same medication. Two messages will be sent during the intervention: The first message will contain the baseline refill score. The second message will note any changes in the refill score.
Treatment:
Behavioral: Messenger effects
Behavioral: Processing fluency
Usual care
No Intervention group
Description:
Participants randomized to this arm will not receive any mailed message.

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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