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NCT07412106Not yet recruiting

Telemedicine-Based Behavioral Intervention to Improve Self-Care Among Hypertensive Patients

Effectiveness of a Telemedicine-Based Behavioral Intervention for Improving Self-Care Practice and Management Outcomes Among Hypertensive Patients Attending Tertiary Hospitals in Northwest Amhara: A Quasi-Experimental Study Intervention Protocol

Source: ClinicalTrials.gov · Last updated 17 Feb 2026

Brief summary (registry, in English)

The goal of this quasi-experimental clinical study is to learn whether a telemedicine-based behavioral intervention can improve self-care practices among adult patients with hypertension receiving care at teaching hospitals in Northwest Amhara. The main questions it aims to answer are: * Does a telemedicine-based intervention improve self-care practices among hypertensive patients? * Does the intervention improve medication adherence among hypertensive patients? * Does the intervention increase patients' knowledge about hypertension? * Does the intervention reduce emergency hospital admissions among hypertensive patients? We will compare patients who receive telemedicine-based counseling with patients who receive usual care to see if the intervention improves self-care, medication adherence, knowledge, and reduces emergency admissions. Participants will: * Receive 10-15-minute telephone counseling sessions every two weeks for three months (intervention group only) * Receive education on blood pressure monitoring, medication adherence, diet, physical activity, and stress management (intervention group only) * Continue routine hypertension care at the hospital (both groups)

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
320 (estimated)
First submitted
31 Jan 2026
Start date
10 Feb 2026
Primary completion date
10 Mar 2026
Lead sponsor
Bahir Dar University
NCT number
NCT07412106

What you commit to

  • Study type: Interventional
  • Planned participants: 320
  • From 10 Feb 2026 to the primary completion date, 10 Mar 2026
  • No sites listed in no 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

  • Participants who have coexisting severe mental health illnesses

Other

  • Severe hearing impairments
  • Pregnant will be excluded

Who the study is looking for

  • Adult patients ≥18 with hypertension who have follow-up for ≥6 months at the study settings
  • Have access to mobile or fixed telephones
  • Will stay for the study follow-up period

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

Full criteria on ClinicalTrials.gov

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