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The effect of follow up using short message service on illness perception and medication adherence in patients under coronary angioplasty

The effect of follow up using short message service on illness perception and medication adherence in patients under coronary angioplasty: a one blind randomized control trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016011025937N1
Enrollment
116
Registered
2016-02-20
Start date
2016-04-03
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

Ischemic Heart Disease. Other forms of chronic ischaemic heart disease

Interventions

Intervention 1: Sending follow-up SMSs for the patients after angioplasty, containing educational subjects, reminders regarding refer time and drug use (five times a week at 10 o’clock in the morning
Sending follow-up SMSs for the patients after angioplasty, containing educational subjects, reminders regarding refer time and drug use (five times a week at 10 o’clock in the morning except Thursdays
routine follow up for control group

Sponsors

Vice Chancellor for Research (VCR) of Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients in range of 18 to 65 years old with diagnosis of acute coronary syndrome referred to Cardiac Clinic of Tabriz University of Medical Sciences; Patients who have gone under angioplasty for at least one month before the study; With the ability to read SMSs; Samples are selected by own tendency; Have a mobile phone and have the ability to use it; Not participating in a similar study like the current one; Exclusion criteria: Not willing to participate in the study; Not having a mobile phone; Referrals to other treatment centers during the study; Not able to read the SMSs; not being accessible after 12 weeks (eg. travelling aboard); Having cognitive impairment, based on patients records

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Illness perception. Timepoint: Before the beginning of intervention and soon as the end of intervention at the end of the third month. Method of measurement: Brief illness perception questionaire.;Medication adherence. Timepoint: Before the beginning of intervention and soon as the end of intervention at the end of the third month. Method of measurement: Morisky medication adherence questionaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Atefeh Allahbakhshian

Tabriz University of Medical Sciences

allahbakhshiana@tbzmed.ac.ir+98 41 3479 6770

Outcome results

None listed

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