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Effect of mobile application on drug use in older adults

An investigation of the drug management application effect on drug adherence and consequences in older adults

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191231045966N1
Enrollment
192
Registered
2021-07-18
Start date
2021-08-23
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Hypertension. Essential (primary) hypertension

Interventions

Intervention 1: Intervention group: The drug application is installed on the intervention group's mobile phone, and reminders about when to take the drugs will be set. Intervention 2: Control group:

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 75 Years

Inclusion criteria

Inclusion criteria: Age between 60-74 years old Conscious consent to enter the study Taking more than five types of medication during the day Reading and writing literacy Having a smart phone and the ability to use it Ability to communicate and not having dementia Having any of the following diseases: hypertension, diabetes, chronic obstructive pulmonary disease (COPD) Use only the drug form of the tablet (Tab) in the drug program

Exclusion criteria

Exclusion criteria: Reluctance to continue participating in the study Hospitalization or death of the participats Use of rare, expensive and special drugs Use of injectable drugs (such as insulin in diabetes)

Design outcomes

Primary

MeasureTime frame
Drug adherence. Timepoint: In the present study, Morisky Adherence Questionnaire (MAQ) will be completed by both control and intervention groups before the start of the study and after 8 weeks from the beginning of the study. Method of measurement: Morisky Adherence Questionnaire (MAQ).

Secondary

MeasureTime frame
Drug consequences. Timepoint: In the present study, a researcher-made questionnaire on drug consequences before and 8 weeks after the intervention will be completed by the control and intervention groups. Method of measurement: researcher-made drug consequences questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahzad Pashaeypoor

Tehran University of Medical Sciences

pashaeypoor.sh@gmail.com+98 912 491 3843

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 10, 2026