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Trial registered on ANZCTR
Registration number
ACTRN12619001618145
Ethics application status
Approved
Date submitted
28/07/2019
Date registered
22/11/2019
Date last updated
22/11/2019
Date data sharing statement initially provided
22/11/2019
Type of registration
Retrospectively registered
Titles & IDs
Public title
Development and Implementation of Pharmacist-based Diabetic Intervention Model in type-2 diabetes patients in Pakistan: A randomized controlled trial
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Scientific title
Development and Implementation of Pharmacist-based Diabetic Intervention Model for patients with type-2 diabetes in Pakistan and impact on Glycated Hemoglobin: A randomized controlled trial
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Secondary ID [1]
298733
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None
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Universal Trial Number (UTN)
U1111-1236-9790
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Trial acronym
PDIM
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Diabetes mellitus
313662
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Condition category
Condition code
Metabolic and Endocrine
312077
312077
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0
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Diabetes
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Around 110 patients will be taken. They will be block randomized into control and intervention group
Pharmacist-based Diabetic Intervention Model (PDIM) includes "Diabetes Educational Module (booklet in both english and local language urdu)", "Medication Adherence improvement strategies" and "tele-pharmacy services" that will be delivered by a Pharmacist, 4 times in a month, at community pharmacy setup.
"Diabetes Educational Module" consists of a booklet that shall be provided to the patient for disease knowledge improvement. This booklet is specifically designed.
Medication improvement adherence strategies shall involve a well designed way of counselling patients, providing drug information by tele-pharmacy services. Subject health, adherence and other self care practice that patient is adopting can be assessed by telephone services for the purpose of follow-up.
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Intervention code [1]
314998
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Treatment: Other
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Intervention code [2]
314999
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Behaviour
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Comparator / control treatment
Subjects shall be allocated to control and intervention by block randomization method.
Control group shall receive no intervention.
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Control group
Active
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Outcomes
Primary outcome [1]
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HbA1C
by Serum assay
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Assessment method [1]
320711
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Timepoint [1]
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180 days
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Primary outcome [2]
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Medication adherence by Morisky Medication Adherence Scale (MMAS)
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Assessment method [2]
320712
0
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Timepoint [2]
320712
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180 days
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Primary outcome [3]
320713
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Health Related Quality of Life
by Euro Qol EQ-5D-5L
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Assessment method [3]
320713
0
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Timepoint [3]
320713
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180 days
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Secondary outcome [1]
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Blood pressure
by using automated machine
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Assessment method [1]
372589
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Timepoint [1]
372589
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180 days
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Secondary outcome [2]
372590
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Lipid Profile (Triglycerides, cholesterol, HDL, LDL)
by serum assay
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Assessment method [2]
372590
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Timepoint [2]
372590
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180 days
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Secondary outcome [3]
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Body Fats
by using Fat analyzer machine
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Assessment method [3]
372591
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Timepoint [3]
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180 days
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Secondary outcome [4]
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BMI
by using fat analyzer machine (Omron Fat analyzer Model: BF508)
A stadiometer will used to assess height in centimeters.
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Assessment method [4]
375060
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Timepoint [4]
375060
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180 days
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Eligibility
Key inclusion criteria
Type-2 diabetes mellitus
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Minimum age
30
Years
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Maximum age
70
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Pregnancy
Juvenile Type Diabetes
Type-1 diabetes
Dementia
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Allocation is not concealed.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computerized Block randomization method in which age, gender, QoL, Adherence score and diabetes facts score will be the co-variates.
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
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Actual
23/09/2019
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Date of last participant enrolment
Anticipated
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Actual
30/09/2019
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Date of last data collection
Anticipated
16/03/2020
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Actual
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Sample size
Target
110
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Accrual to date
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Final
110
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Recruitment outside Australia
Country [1]
21686
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Pakistan
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State/province [1]
21686
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Punjab
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Funding & Sponsors
Funding source category [1]
303287
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Government body
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Name [1]
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Higher Education Commission
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Address [1]
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H-9/4 H 9/4 H-9, Street 3, Islamabad, Islamabad Capital Territory
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Country [1]
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Pakistan
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Primary sponsor type
Individual
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Name
Tauqeer Hussain
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Address
Department of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Government College University, Kotwali Road, Gurunanakpura, Faisalabad-38000, Punjab
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Country
Pakistan
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Secondary sponsor category [1]
303306
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Individual
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Name [1]
303306
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Malik Hassan Mehmood
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Address [1]
303306
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Department of Pharmacology, Faculty of Pharmaceutical Sciences, Government College University, Kotwali Road, Gurunanakpura, Faisalabad-38000, Punjab
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Country [1]
303306
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Pakistan
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Other collaborator category [1]
280853
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Individual
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Name [1]
280853
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Mustafa Ijaz
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Address [1]
280853
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Faculty of Pharmaceutical Sciences, Government College University, Kotwali Road, Gurunanakpura, Faisalabad-38000, Punjab
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Country [1]
280853
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Pakistan
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Other collaborator category [2]
280854
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Individual
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Name [2]
280854
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Zulqarnain Haider
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Address [2]
280854
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Department of Pharmacology, Faculty of Pharmaceutical Sciences, Government College University, Kotwali Road, Gurunanakpura, Faisalabad-38000, Punjab
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Country [2]
280854
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Pakistan
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
303823
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Institutional Ethical Committee of Government College University Faisalabad
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Ethics committee address [1]
303823
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Government College University, Allama Iqbal Road. Faisalabad Pakistan
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Ethics committee country [1]
303823
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Pakistan
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Date submitted for ethics approval [1]
303823
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31/07/2019
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Approval date [1]
303823
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01/08/2019
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Ethics approval number [1]
303823
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GCUF/ERC/2065
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Summary
Brief summary
The study is designed as prospective, randomized controlled trial. In this study, around 110 patients shall be screened and allocated into groups based upon block randomization method. Pre- and Post-Intervention data from subjects shall be recorded on prestructured data collection form and the time between these two points shall be of 6 months. Intervention includes education about disease and treatment. The impact of this intervention on HbA1C and the secondary outcomes like BMI, visceral fats and body fats shall be determined.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Tauqeer Hussain Mallhi
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Address
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Department of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Government College University, Kotwali Road, Gurunanakpura, Faisalabad-38000, Punjab
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Country
94934
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Pakistan
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Phone
94934
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+923007600072
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Fax
94934
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Email
94934
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[email protected]
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Contact person for public queries
Name
94935
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Mustafa Ijaz
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Address
94935
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Faculty of Pharmaceutical Sciences, Government College University, Kotwali Road, Gurunanakpura, Faisalabad-38000, Punjab
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Country
94935
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Pakistan
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Phone
94935
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+923357393376
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Fax
94935
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Email
94935
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[email protected]
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Contact person for scientific queries
Name
94936
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Tauqeer Hussain Mallhi
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Address
94936
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Department of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Government College University, Kotwali Road, Gurunanakpura, Faisalabad-38000, Punjab
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Country
94936
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Pakistan
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Phone
94936
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+923007600072
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Fax
94936
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Email
94936
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
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What data in particular will be shared?
All of the data
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When will data be available (start and end dates)?
9/23/2019-9/23/2021
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Available to whom?
Researchers only
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Available for what types of analyses?
any purpose
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How or where can data be obtained?
by email application to principal investigator or primary sponsor
[email protected]
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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