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SMS and reminder cards for improving medication adherence

A comparison between the effectiveness of short message service and reminder cards regarding medication adherence in patients with hypertension: A randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015110917059N2
Enrollment
143
Registered
2015-12-13
Start date
2014-03-03
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

hypertension. Essential (primary) hypertension, Secondary hypertension

Interventions

Intervention 1: Intervention group 1: In the reminder cards group, cards in four different colors with the content of the medication regimen (30 cards), diet (30 cards), physical activities (30 cards)
Treatment - Drugs
Intervention group 1: In the reminder cards group, cards in four different colors with the content of the medication regimen (30 cards), diet (30 cards), physical activities (30 cards) and blood press
Intervention group 2: The patients in the text messaging group will be sent 6 messages a week. Educational content of text messaging is same to educational content of reminder cards and contains medic

Sponsors

Vice chancellor for research, Urmia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Major inclusion and exclusion criteria: Uncontrolled hypertension confirmed by doctor; being on medication for hypertension; living in the city of Urmia; having access to a mobile phone in patient or a member of his family; being able to use the text messaging function in patient or a member of his family (reading and composing a text message); not being on medication for prostate in the male patients; and willingness to participate in the study will be entry requirements. The exclusion criteria will be: being hospitalized in the duration of the study, unwillingness to participate further; moving to another city; and loss of contact with the patient through his/her mobile phone.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Adherence to treatment. Timepoint: Two times. Method of measurement: Hill-Bone medication adherence scale.

Secondary

MeasureTime frame
Hypertension. Timepoint: Two times. Method of measurement: Mercury sphygmomanometer.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026