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Piloting Text Messages to Promote Positive Affect and Physical Activity

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Mass General Brigham

Status

Completed

Conditions

Acute Coronary Syndrome

Treatments

Behavioral: Intervention arm: Text Message Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT04077229
2016P001472

Details and patient eligibility

About

The focus of the study is to assess the feasibility and acceptability of a pilot one-arm project delivering text messages related to positive psychology (PP) activities (e.g., recalling positive events) and health behavior text messages (e.g. having a heart-healthy diet, becoming more physically active). The messages will be sent for 4 weeks among patients with a prior acute coronary syndrome (ACS).

Full description

This is a single-arm study of text messaging in post-ACS patients. The convenience sample for this pilot study will be enrolled from two sources: (a) participants prospectively enrolled from inpatient cardiac units at MGH admitted for an ACS, and (b) participants in prior post-ACS studies performed with the investigators' team.

A total of 28 intervention text messages (1/day for 4 weeks) will be sent to participants following the baseline assessment. After each message is sent, participants will receive a second text message asking them to rate the utility of the message, and this rating will be used by a machine learning algorithm to select subsequent messages. This will ensure that, over time, participants will receive messages that they are more likely to find useful.

In the first part of the study, participants will receive 28 fixed text messages that alternate between physical activity and positive psychology messages. In the second part of the study, participants will receive 14 fixed text messages that range in topics from positive psychology to physical activity, diet, and medication adherence. In the second part of the study, participants will first receive a set of 14 pre-selected daily messages that contain a broad range of attributes to allow sufficient participant feedback to clearly identify preferences. After the first 14 messages, new messages will be selected based on the prior preferences of participants.

The messages will be sent using the Twilio texting program used by REDCap, which also uses Amazon Web Services. Twilio allows software developers to programmatically make and receive phone calls and send and receive text messages using its web service. The investigators have purchased a Twilio account to allow messages to come from an anonymous phone number rather than the phone of a study staff member.

Enrollment

63 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Prior acute coronary syndrome.

    Acute myocardial infarction (MI):

    • Elevation of cardiac biomarkers (cardiac troponin T) in addition to one or more of the following:
    • symptoms of ischemia (e.g., acute chest pain)
    • ischemic changes on electrocardiogram
    • imaging evidence of new loss of viable myocardium or new regional wall motion abnormality.

    Unstable angina (UA):

    • crescendo angina
    • new onset (within 1 month) angina with minimal exertion
    • angina with minimal exertion or at rest.
  2. Ability to receive text messages via cellular phone.

Exclusion criteria

  • A periprocedural ACS
  • Terminal illness
  • An unrelated condition limiting physical activity
  • An inability to communicate in English, or
  • cognitive disorder assessed by 6-item cognitive screen

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

63 participants in 1 patient group

Intervention
Experimental group
Description:
A total of 28 intervention text messages (1/day for 4 weeks) will be sent to participants following the baseline self-report assessment. After each message is sent, participants will receive a second text message asking them to rate the utility of the message. Following the 4-week intervention, participants will complete the same self-report assessments as in the baseline assessment (via phone) and will provide feedback about the program. Finally, 4 weeks later (at 8 weeks), participants will repeat the self-report questionnaires by phone.
Treatment:
Behavioral: Intervention arm: Text Message Intervention

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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