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Evaluating the Effectiveness of Education Session by Pharmacists in Patients with Asthma

A Randomized Controlled Trial Evaluating the Effectiveness of Education Session by Pharmacists in Patients with Asthma in Indonesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20171219001
Enrollment
100
Registered
2017-12-19
Start date
2017-08-28
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Patients with asthma diagnosed asthma&#44

Interventions

The trial evaluates an intervention involving pharmacists to deliver one&#45
one education session about: (1) asthma medication that has been used (2) how to use asthma medication devices correctly (3) asthma symptoms and how to prevent the asthma exacerbations and (4) how to
how to recognize worsening asthma&#44
what to do when symptoms are getting worse and what to do in the event of an acute attack&#44
including a first aid plan,Participants allocated to the control group received the usual medical care provided by the Department of Pulmonology and/or their healthcare professionals. This included th
it was apparent that their asthma control had deteriorated since prior assessment (for example
using their reliever two or more times a week&#44
needing to increase their preventer dose)&#44
the participant and her health professionals will be notified with participant’s permission.
Experimental Other,No Intervention Other
Education session by pharmacist,Usual Care

Sponsors

Ministry of Technology and Higher Education of Indonesia
Lead Sponsor
Ministry of Technology and Higher Education of Indonesia
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Eligibility for this trial included patients with asthma who had used any regular medications for asthma within the previous 12 months, aged 18 years or older and able to communicate in Indonesian.

Exclusion criteria

Exclusion criteria: Those who are not able or contra indicated to perform lung function with spirometer will be excluded.

Design outcomes

Primary

MeasureTime frame
Changes in asthma control baseline and every 1, 2 and 3 months Asthma Control Questionnaire (ACQ)

Secondary

MeasureTime frame
Changes in Asthma Quality of Life baseline and every 1, 2 and 3 months Asthma Quality of Life Questionnaire (AQLQ) ,Forced Expiratory Volume in 1 second (FEV1) baseline and every 1, 2 and 3 months Spirometer,asthma-related health visits, days off work/study, and oral corticosteroid use baseline and at 3 months Questionnaire and patient medical records,Adherence score baseline and every 1, 2 and 3 months Adherence to Refills and Medications Scales (ARMS) questionnaire

Countries

Indonesia

Contacts

Public ContactElida Zairina

Universitas Airlangga

elida-z@ff.unair.ac.id625020514

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026