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NCT06951451Enrolling by invitation

Effect of Smartphone Application (MED-AD) on Medication Adherence Among Patients With Cardiovascular Disease in Oman

Effect of Smartphone Application (MED-AD) on Medication Adherence Among Patients With Cardiovascular Disease in Oman: A Multicenter Randomized Clinical Trial

Source: ClinicalTrials.gov · Last updated 30 Apr 2026

Brief summary (registry, in English)

This study aims to: 1. Investigate the impact of MED-AD intervention on medication adherence among CVD patients, compared to patients receiving text message reminders or routine care alone at baseline, 6 months, and 12 months later. 2. Evaluate the effectiveness of MED-AD intervention on clinical outcomes among patients with CVD, compared to the outcomes of patients receiving text or routine care alone at baseline, 6 months, and 12 months later. This study is a prospective randomized controlled clinical trial (RCT) with three arms: 1. MED-AD intervention: MED-AD is a smartphone application that will use the following strategies (pill reminders, Medication Adherence Report, medication intake confirmation, Medical Appointment Reminder, and educational notifications) to enhance medication adherence 2. Text message reminders: Participants will receive short text message (SMS) reminders to remind them to take medications as prescribed once daily 3. Routine care only: Participants will receive routine care that does not include text messages or reminders and education through an application.

Status (registry)
Enrolling by invitation
Study type
Interventional
Enrollment
1000 (estimated)
First submitted
20 Apr 2025
Start date
1 Jun 2025
Primary completion date
28 Jun 2026
Lead sponsor
Sultan Qaboos University
NCT number
NCT06951451

What you commit to

  • Study type: Interventional
  • Planned participants: 1000
  • From 1 Jun 2025 to the primary completion date, 28 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • have a severe cognitive impairment,

Other

  • are unable to provide informed consent,
  • cannot read, and 4) do not have a smartphone with a compatible operating system (ios or Android).

Who the study is looking for

  • diagnosed with at least one CVD (i.e., HTN, IHD, hyperlipidemia),
  • prescribed at least one medication for at least one year,
  • Omanis aged 18 years or older,
  • registered in the selected healthcare center, and 5) agreed to participate in the study

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ministry of Health
Coordinator of this site? Confirm its status
MuscatOmanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.