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Asthma Control Through Telemedicine (PLET-I)

H

Hamdard University

Status

Not yet enrolling

Conditions

Asthmatic Patients

Treatments

Other: Educational

Study type

Interventional

Funder types

Other

Identifiers

NCT06863285
ABJan012025

Details and patient eligibility

About

The purpose of this research study is to evaluate the impact of pharmacist led educational interventions on Asthmatic patients, and also determine their medication adherence.

Pharmacist's intervention aims to answer:

  1. How a pharmacist intervention program impact medication adherence in persistent asthma?
  2. To assess how pharmacist led educational intervention like patients' counseling and medication reminders through Telemedicine have an impact on patient's asthma control?
  3. Which mode of communication (Verbal instructions, videos and pamphlets) for the patient counselling is most beneficial for the patients in asthma control.

Full description

This is a randomized, pharmacist-led, two-group, longitudinal descriptive interventional study performed through in person (Public and private hospitals) and telecommunication (WhatsApp, network calls and messaging). The investigator will use snowball method to approach patients through telecommunication. Recruited patients will be randomly divided into two groups: the Control and the experimental group. The Control Group will not receive any intervention, and experimental group will receive special counseling about persistent asthma, it's medications and medical devices, their appropriate use, and side effects. Using Telemedicine as message and call reminders to increase medication adherence and improve their asthmatic condition. The intervention will be conducted for one month on the experimental group according to the recruitment date and time of the patients.

Pre-validated questionnaires will be used for the assessment

  1. The adherence to asthma medication questionnaire (AAMQ-13).
  2. Asthma Control test TM (ACT).

Enrollment

140 estimated patients

Sex

All

Ages

11+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age above 11 years.
  • Persistent Asthma Patient.
  • Patients taking medications and inhaler.
  • Patient who will consent for the study.
  • Patient with basic telecommunication facility.
  • Patient who responded to messages and calls.

Exclusion criteria

  • Patients who will refuse to participate in study will not be included.
  • Irresponsive patients to messages and calls

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

140 participants in 2 patient groups

Study group
Experimental group
Description:
intervention included the usual counselling by pharmacist e.g. Patients Education regarding Medications * Pharmacist counseling patients regarding their disease and severity * Pharmacist counseling (5- to 10-minute sessions) on the proper and safe use of medication. * Pharmacist counseling patients regarding the importance of their therapy (treatment), non-pharmacological treatment like diet and exercises. pharmacist counselling regarding the preventive measures that prevent patient from triggers that can initiate asthmatic attacks.
Treatment:
Other: Educational
Control group
No Intervention group
Description:
No intervention

Trial contacts and locations

1

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Central trial contact

MUhammad Abubakar, PhD; Matti Ullah, PhD

Data sourced from clinicaltrials.gov

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