- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04412239
To Assess the Efficiency and Satisfaction of Pharmacist Giving Patient-centred Advice on Telephone Consultation in TB Patients: Experience of the COVID-19 Pandemic (Coronavirus19)
November 16, 2020 updated by: Farman Ullah Khan, Health Science Center of Xi'an Jiaotong University
The COVID-19 pandemic might be an opportunity to review and refine our practices in anti TB treatment.
For the follow-up of selected patients, telephone consultations may be efficient and cost-effective.
The aim of the study is to assess the efficiency and the satisfaction with telephone consultation for the pharmacist and the TB patient.
The study was conducted in tertiary care hospital TB control centres patients.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Tuberculosis (TB) is the world's biggest killer among infectious diseases, claiming more than 4000 lives each day.
The unprecedented coronavirus pandemic seriously impacts people with pre-existing health conditions.
People who have TB are usually more vulnerable to other infections, including the novel coronavirus, due to pre-existing lung damage.
They are at a higher risk of developing complications from COVID-19.
Certain populations are at greater risk of TB, because of where they live, where they work or because of other socio-economic factors which result in them experiencing barriers to accessing health services.
Study Type
Interventional
Enrollment (Anticipated)
200
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
KPK
-
Bannu, KPK, Pakistan, 2800
- Recruiting
- Dhq Bannu Kpk
-
Contact:
- Farman Ull ah Khan
- Phone Number: +92331-3319443131
- Email: farmankhan@bs.qau.pk
-
Bannu, KPK, Pakistan, 2800
- Recruiting
- District Bannu TB Control Center
-
Contact:
- Asif Ul Khan, Master
- Phone Number: 0092334087008
- Email: asifkhanustb@gmail.com
-
Principal Investigator:
- Farman Ul Khan, Master
-
Sub-Investigator:
- Yu Fang, Phd
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
New, smear-positive drug-susceptible TB who have been on treatment for less than two weeks Access to a mobile phone (self-reported)
Exclusion Criteria:
Patients who do not have regular access to a mobile phone Patients who have previously received TB treatment Patients who have another member in their household who is already a part of the study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Telephone Consultation in TB Patients
The COVID-19 pandemic might be an opportunity to review and refine our practices in TB care.
For the follow-up of selected patients, telephone consultations may be efficient and cost-effective.
|
The primary aim was to assess the efficiency and the satisfaction of the telephone consultation.
The COVID-19 pandemic might be an opportunity to review and refine our practices in TB care.
For the follow-up of selected patients, telephone consultations may be efficient and cost effective.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Efficiency of the telephone consultation,
Time Frame: 2 Months
|
To improve patient centered care/patient prescription refill
|
2 Months
|
|
Patient satisfaction
Time Frame: 2 Month
|
Patient satisfaction Patient satisfaction resulting from pharmacist-led pharmaceutical care will be assessed Patient satisfaction feedback (PSF)
|
2 Month
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Adherence Rate
Time Frame: 2 Months
|
2 Months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 20, 2020
Primary Completion (Anticipated)
December 20, 2020
Study Completion (Anticipated)
December 20, 2020
Study Registration Dates
First Submitted
May 30, 2020
First Submitted That Met QC Criteria
May 30, 2020
First Posted (Actual)
June 2, 2020
Study Record Updates
Last Update Posted (Actual)
November 18, 2020
Last Update Submitted That Met QC Criteria
November 16, 2020
Last Verified
November 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Coronavirus Infections
- Coronaviridae Infections
- Nidovirales Infections
- RNA Virus Infections
- Virus Diseases
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Pneumonia, Viral
- Pneumonia
- Lung Diseases
- Bacterial Infections
- Bacterial Infections and Mycoses
- Gram-Positive Bacterial Infections
- Actinomycetales Infections
- Mycobacterium Infections
- COVID-19
- Tuberculosis
Other Study ID Numbers
- NO, F6-2017/NTP-ADMIN
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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