Evaluation of Lifestyle Education and Events Via Network Text Messages After Acute Coronary Syndrome
Elena
1 other identifier
interventional
370
1 country
1
Brief Summary
To evaluate the usefulness of telephone text messages (TTM) in the control of risk factors and in the reduction of events in the first year after an ACS (acute coronary syndrome).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started May 2019
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2023
CompletedFirst Submitted
Initial submission to the registry
December 28, 2025
CompletedFirst Posted
Study publicly available on registry
January 9, 2026
CompletedJanuary 9, 2026
December 1, 2025
3.8 years
December 28, 2025
December 28, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Composite of cardiac death, myocardial infarction, stroke or new revascularization
Occurrence of Composite of cardiac death, myocardial infarction, stroke or new revascularization
12 months
Secondary Outcomes (14)
Systolic blood pressure (SBP) mm Hg
12 months
Diastolic blood pressure (DBP) (mm Hg)
12 months
Change in Weight (kilograms)
12 months
Low Density Lipoproteins (LDL) cholesterol (mg/dl)
12 months
High (HDL) cholesterol (mg/dl)
12 months
- +9 more secondary outcomes
Study Arms (2)
Text messaging group with usual care
EXPERIMENTALUsual Care
ACTIVE COMPARATORInterventions
The patient received a monthly telephone text messages (TTM) for 12 months with the recommendations of the Spanish Society of Cardiology regarding secondary prevention and followed the usual review protocol in a specific ischemic heart disease consultation at 3 and 12 months after discharge.
The patient received followed the usual review protocol in a specific ischemic heart disease consultation at 3 and 12 months after discharge.
Eligibility Criteria
You may qualify if:
- Patients discharged with ACS and without ST elevation.
- Informed consent signed.
You may not qualify if:
- Refusal to participate in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Fundación EPIClead
Study Sites (1)
Hospital Universitario de Cabueñes
Cabueñes, Spain
Related Publications (5)
Free C, Phillips G, Galli L, Watson L, Felix L, Edwards P, Patel V, Haines A. The effectiveness of mobile-health technology-based health behaviour change or disease management interventions for health care consumers: a systematic review. PLoS Med. 2013;10(1):e1001362. doi: 10.1371/journal.pmed.1001362. Epub 2013 Jan 15.
PMID: 23349621BACKGROUNDSharma P APMptm, in fpatat, en/ pwHiRchawirhacsc, 2015). aF.
BACKGROUNDAnglada-Martinez H, Riu-Viladoms G, Martin-Conde M, Rovira-Illamola M, Sotoca-Momblona JM, Codina-Jane C. Does mHealth increase adherence to medication? Results of a systematic review. Int J Clin Pract. 2015 Jan;69(1):9-32. doi: 10.1111/ijcp.12582. Epub 2014 Dec 4.
PMID: 25472682BACKGROUNDAdler AJ, Casas JP, Martin N, Free C, Perel P. Cochrane corner: text messaging to improve adherence to drugs for secondary prevention of cardiovascular disease. Heart. 2018 Nov;104(22):1814-1816. doi: 10.1136/heartjnl-2017-312888. Epub 2018 May 14. No abstract available.
PMID: 29760242BACKGROUNDSenatore FF, Califf RM. Standardized classification and framework for reporting and interpreting medication non-adherence in clinical trials. Eur Heart J. 2019 Jul 1;40(25):2086-2088. doi: 10.1093/eurheartj/ehy759. No abstract available.
PMID: 30496403BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 28, 2025
First Posted
January 9, 2026
Study Start
May 1, 2019
Primary Completion
February 1, 2023
Study Completion
March 1, 2023
Last Updated
January 9, 2026
Record last verified: 2025-12