Skip to content

Impact of Pharmacist intervention on asthma management

Impact of Pharmacist intervention in Asthma control: A Parallel Group Randomized Controlled Trial in Outpatients

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625000661471
Enrollment
150
Registered
2025-06-23
Start date
2025-07-01
Completion date
2025-09-01
Last updated
2025-09-08

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

Conditions

None listed

Brief summary

This study aims to assess the impact of pharmacist-led interventions on asthma management, medication adherence, and health-related quality of life (HRQoL). A randomized controlled trial will be conducted at a Fatima Jinnah chest hospital in Quetta with 150 asthmatic patients divided equally into control and intervention groups. The intervention group will receive personalized education and support from pharmacists, while the control group will receive standard care. Outcome measures will be assessed at baseline, month 3, and month 6 using validated tools, and analyzed using SPSS. Positive results could support a greater role for pharmacists in managing chronic diseases in Pakistan

Interventions

All eligible clinically diagnosed asthma outpatients receiving regular treatment at Fatima Jinnah Institute of Chest Diseases, Quetta, Balochistan will be included in the study. A pharmacist trained in the pathophysiology, management of asthma, and use of the current study protocol will administer the intervention. The intervention will include one-on-one sessions. There will be 2 sessions of one hour per week and sessions will continue for 6 weeks (with proper marked attendance of patients for

All eligible clinically diagnosed asthma outpatients receiving regular treatment at Fatima Jinnah Institute of Chest Diseases, Quetta, Balochistan will be included in the study. A pharmacist trained in the pathophysiology, management of asthma, and use of the current study protocol will administer the intervention. The intervention will include one-on-one sessions. There will be 2 sessions of one hour per week and sessions will continue for 6 weeks (with proper marked attendance of patients for each session) during which pharmacist will educate the patient on basic facts about asthma, understanding difference between the controller and reliever medications, taking medications correctly, correct use of inhaler, spacer, nebulizer etc., identifying and avoiding environmental exposure that exacerbate asthma, self-monitoring to assess the level of asthma control, monitor and recognize early signs and symptoms of worsening asthma, and provide written action plans to know when and how to take daily actions to control asthma, adjust medications in response to signs of worsening asthma, and when to seek medical care. Written Action Plan, developed by the National Institutes of Health (NIH), will be provided to each patient. This action plan will include detailed instructions on daily actions to control asthma, how to adjust medications in response to changing symptoms, and when to seek medical care. Patients will be taught how to write and personalize their own action plan, ensuring they can monitor their asthma and adjust treatments effectively. Patient outcomes, including inhaler technique, asthma control, quality of life, and medication adherence, will be measured using the 11 items checkpoint of inhaler technique (WHO), Asthma Control Questionnaire (ACQ), the Asthma Quality of Life Questionnaire (AQLQ), and the General Medication Adherence Scale (GMAS), respectively. These tools are available in Urdu, and permission has been granted to use them in their authorized version and self designed data collection form will be used. This comprehensive program will empower patients to manage their asthma effectively and make informed decisions about their health.

Sponsors

University of Balochistan
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

Outpatients diagnosed with asthma aged 18 years and above Receiving asthma medication for the past 6 months at least

Exclusion criteria

Patients who cannot understand and read Urdu. Pregnant patients. Patients unable to communicate. Patients with comorbidities affecting asthma management e.g. patients with chronic obstructive pulmonary disease (COPD). Patient with a documented chest infection in the last four weeks

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026