ClinicalTrials.gg
CompletedNCT07878728Updated Oct 26, 2026

Text Message Support to Help Adults With Newly Diagnosed High Blood Pressure Control Their Blood Pressure in Primary Care Clinics in Germany and Pakistan

An interventional study of mHealth Text Message Program and Usual Care in Hypertension and Primary Hypertension, sponsored by GIFT University. Completed at 1 site in Pakistan. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-26.

Sponsored by GIFT University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 6 months after the study started (first participant enrolled Apr 2025, registered Oct 2026).
Updated Oct 26, 2026Eligibility revisedNewly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
1,295
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this clinical trial is to learn if text messages can help adults with newly diagnosed high blood pressure (hypertension) bring their blood pressure under control. The study took place in primary care clinics in Bangladesh and Pakistan. The main questions it aims to answer are:

Do more participants who get text messages have their blood pressure under control after 6 months? Under control means a top number below 140 and a bottom number below 90.

Do text messages help participants take their blood pressure medicine as prescribed?

Researchers compared a text message program to usual care to see if the text messages work to lower blood pressure. They randomly assigned whole clinics, not individual people, to one of the two groups.

Participants:

Got text messages for 6 months, or got written health materials and usual care. Received daily messages for the first month and fewer after that, if in the text message group. The messages encouraged taking medicine, healthy habits, and checking blood pressure.

Had their blood pressure checked at 9 weeks and at 6 months.

Read the detailed description

Hypertension is a major risk factor for heart disease and death worldwide, and it can be treated. But many people with hypertension still do not reach healthy blood pressure levels. This trial tests whether a low-cost text message program can help adults with newly diagnosed hypertension reach blood pressure control in routine primary care.

The trial is multicenter and cluster randomized. Researchers randomly assigned whole primary care clinics, rather than individual participants, to the text message program or usual care. Clinics were assigned in a 2:1 ratio, so twice as many clinics offered the text message program as usual care. Participants were followed for 6 months.

Blood pressure control was the main focus because it is the clinical goal of hypertension treatment. The trial also looked at several other measures of how participants did on treatment. These include blood pressure control at an earlier point (9 weeks), how long participants stayed on their medicine, whether treatment worked or failed, how many participants dropped out of follow-up, and deaths.

Because participants in the same clinic may have similar outcomes, the analysis accounts for clustering by clinic.

02

Conditions studied

  • Hypertension
  • Primary Hypertension

Keywords

  • mHealth
  • Mobile health
  • Text messaging (SMS)
  • Blood pressure control Medication adherence
  • Lifestyle modification
  • Primary care
  • Cluster randomized trial
  • Low- and middle-income countries
  • Digital health
03

In context

Hypertension

6,834 studies on the registry are indexed under Hypertension; 971 are open to participants now.

This study's enrollment of 1,295 is above the median of 90 across 5,095 interventional studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

GIFT University is the lead sponsor of 8 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 18 years or older
  • Diagnosed with primary hypertension within the past 4 weeks
  • Receiving care at one of the participating primary care clinics

Exclusion criteria

Exclusion Criteria

  • Secondary hypertension
  • Recent major cardiovascular event (stroke or heart attack)
  • Enrolled in another blood pressure management study or another interventional study
  • Serious health conditions that could interfere with participation or with measuring outcomes
  • Unable to understand study procedures
  • Unable to communicate with researchers by mobile phone
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,295 participants (actual)

Study arms

  • Experimental
    mHealth Text Message Program

    Participants receive text messages for 6 months that encourage taking blood pressure medicine, making healthy lifestyle changes, and checking blood pressure. Messages are sent daily for the first month and less often after that. Participants also receive routine hypertension care at their clinic.

    Behavioral: mHealth Text Message Program

  • Active comparator
    Usual Care

    Participants receive written educational materials about hypertension and routine hypertension care at their clinic for 6 months. They do not receive text messages.

    Other: Usual Care

Interventions

  • BehavioralmHealth Text Message Program

    Participants receive text messages on their mobile phones for 6 months. The messages encourage three things: taking blood pressure medicine as prescribed, making healthy lifestyle changes, and checking blood pressure. Messages are sent daily for the first month and less often after that. Participants receive this program in addition to routine hypertension care at their clinic.

  • OtherUsual Care

    Participants receive written educational materials about hypertension and routine hypertension care at their clinic for 6 months. They do not receive text messages.

06

What researchers measure

Primary outcomes

  1. Blood pressure control at 6 months

    Percentage of participants whose blood pressure is under control at 6 months. Control means systolic blood pressure (the top number) below 140 mm Hg and diastolic blood pressure (the bottom number) below 90 mm Hg.

    Time frame: 6 months

Secondary outcomes

  1. Blood pressure control at 9 weeks

    Percentage of participants whose blood pressure is under control at 9 weeks. Control means systolic blood pressure (the top number) below 140 mm Hg and diastolic blood pressure (the bottom number) below 90 mm Hg.

    Time frame: 9 weeks

  2. Treatment adherence

    Number of days participants take their blood pressure medicine during the 6-month follow-up.

    Time frame: 6 months

  3. Treatment success

    Percentage of participants who have treatment success at 6 months.

    Time frame: 6 months

  4. Treatment failure

    Percentage of participants who have treatment failure during the 6-month follow-up.

    Time frame: 6 months

  5. Loss to follow-up

    Percentage of participants who stop attending follow-up visits and cannot be assessed during the 6-month follow-up.

    Time frame: 6 months

07

Study locations

1 site
  • Gujranwala Institute of Future Technologies
    Multan Khurd, Punjab, Pakistance 60000, Pakistan
08

References and documents

Individual participant data

Plan to share: Undecided — The research team has not yet decided whether to share individual participant data (IPD) with other researchers. A decision will be made after the main results are published. Any plan will follow the ethics approvals and consent terms of the participating clinics.

No publications or documents are linked to this record.

09

Updates

2 registry updates since Sep 25, 2026
Also revised
eligibility
Registered
First appeared on the registry
Oct 16, 2026
Show all 2 updates
  1. Oct 26, 2026
    Eligibility Criteria revised
  2. Oct 16, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07878728
Lead sponsor
GIFT University
Responsible party
Amna Iqbal (Principal investigator, Bahauddin Zakariya University) — Principal investigator
First posted
Oct 16, 2026
Start date
Apr 8, 2025
Primary completion
Jun 8, 2025
Completion
Sep 11, 2025
Last update
Oct 26, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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