Skip to content

Efficacy of Education Via Phone-based Text Messaging (SMS) on Patients With Uncontrolled Hypertension

Efficacy of Education Via Phone-based Text Messaging (SMS) on Patients With Uncontrolled Hypertension: a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05711004
Enrollment
200
Registered
2023-02-02
Start date
2023-10-01
Completion date
2024-03-01
Last updated
2023-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Brief summary

Uncontrolled hypertension (HTN) is a major public health worldwide, which increases the risk of cardiovascular diseases. Low adherence to medication, unhealthy lifestyle and poor knowledge of HTN diagnosis and treatment are among the known factors associated with uncontrolled HTN. Digital innovations became popular as low-cost tools to provide personalized advice to people with long-term health conditions, leading to their adherence to health behavior modifications. Therefore, this randomized single-blind controlled trial (RCT) aimed to test whether providing health information via a short message service (SMS) influences blood pressure control, health practice, and medication adherence. For the current RCT, the investigators will use data from the PERSIAN Kavar cohort study (PKCS). Eligible participants with uncontrolled HTN will be randomly assigned to experiment (SMS) or control (routine care) groups at a 1:1 ratio. Participants in the experimental group will receive three messages/per week for three months. Systolic and diastolic blood pressure will be the primary outcomes of this study. Medication adherence and practice related to cardiovascular diseases will the secondary outcomes. These variables will be assessed before and after the intervention. At the end of the study, the acceptability of the messages will also be assessed.

Interventions

BEHAVIORALEducation via SMS

Participants in the experimental group will receive three messages per week in the morning (9-10 am) for three months. The investigators will call them every month to ensure that the SMS is delivered.

Sponsors

Shiraz University of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Intervention model description

Eligible participants with uncontrolled HTN will be randomly assigned to experiment (SMS) or control (routine care) groups at a 1:1 ratio.

Eligibility

Sex/Gender
ALL
Age
35 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients who have a diagnosis of HTN by a clinician at the baseline or until the third follow-up of PKCS, have uncontrolled HTN (≥140/90) at the enrollment, have a prescription for blood pressure-lowering medication, understand Persian, have regular access to a mobile phone, and are able to read SMS by themselves or with their family's help. The investigators will enroll only one member per household.

Exclusion criteria

* Those with renal failure or requiring specialist care for their hypertension at a hospital, pregnant women or who are within 3 months postpartum, patients with severe physical or mental illness, and subjects not willing to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
Blood pressureThree months after the start of interventionSystolic and diastolic blood pressure

Secondary

MeasureTime frameDescription
Medication adherence which will be assessed by Morisky Medication Adherence ScaleThree months after the start of interventionAdherence to the anti-HTN drugs will be assessed by Morisky Medication Adherence Scale .
Practice according to the KAP questionnaireThree months after the start of interventionThe questions of Knowledge, Attitude, and Practice Regarding Cardiovascular Diseases (doi: 10.5812/ijem.101612) questionnaire that are related to Practice will be completed for patients.
WeightThree months after the start of interventionBody weight (kg)
Number of patients who think that messages were usefull and had positive impactThree months after the start of interventionAcceptability of the messages will be assessed according to the questiones listed in doi: 10.5334/gh.1103

Contacts

Primary ContactAli Reza Safarpour, Ph.D.
safarpourar@gmail.com+98-7136281442
Backup ContactSara Shojaei-Zarghani, Ph.D.
shojaeisara@ymail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026