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Impact of Clinical Pharmacist-Led Intervention on Management of Diabetic Hypertensive Patients in Eastern Nepal

Primary Purpose

Type 2 Diabetes, Hypertension

Status
Recruiting
Phase
Not Applicable
Locations
Nepal
Study Type
Interventional
Intervention
Clinical Pharmacist-Led Educational Intervention
Sponsored by
Chettinad Academy of Research and Education (Deemed to be University)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Type 2 Diabetes

Eligibility Criteria

40 Years - 68 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Male and female patients aged 40 to 68 years. Clinically diagnosed with type II diabetes mellitus with hypertension as co-morbidity. Minimum one year of the medical history of diabetic and hypertension. Minimum 6 months on antidiabetic as well as antihypertensive medication therapy. Patients willing to participate in the study and those providing written informed consent for participation. Exclusion Criteria: Patients with Type I diabetes mellitus, Diabetic insipidus, Gestational diabetes or other forms of diabetes. Presence of other chronic disease co-morbidity other than hypertension and diabetes complications. Mentally incompetent patients, Pregnant, critically ill patients (requiring hospital admission). Patients have tuberculosis, Corona virus, and other highly communicable diseases. Those patients not willing to performing routine follow-up visit.

Sites / Locations

  • Purbanchal University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Other

Arm Label

Control group (Usual Standard Care)

Intervention Group (Clinical Pharmacist-led educational Intervention)

Arm Description

Control group patient will undergo routine care by their physician and nurses. However, the investigator will only provide basic counseling regarding drug prescribed during discharge to the patients. In another term "Usual care" will be provided to the patients

In addition to routine care by physician and nurses, Patients in interventional group will receive two consecutive face to face interview and counseling of 20-40 minutes during the baseline period and the first follow-up period at 3-month by clinical pharmacist. Teaching and counseling session involves information on various non-pharmacological and pharmacological disease management strategies.

Outcomes

Primary Outcome Measures

Change in blood pressure
Assessed with measurement of Systolic and diastolic blood pressure in mmHg using sphygmomanometer
Change in blood glycemic profile
Assessed with measurement of Fasting Blood Sugar (FBS) and Post Prandial Blood Sugar (PPBS) in mg/dl.
change in glycosylated hemoglobin (HbA1C) level
assessed from patients glycosylated hemoglobin (HbA1C) level test, measured in percent (%)
Impact of Intervention in Patients Medication Adherence
It will be measured using translated and validated Nepalese version of the 11-item Novel general medication adherence Scale (GMAS) questionnaire divided into three categories based on a four-level Likert scale. GMAS tools provide a wide range of components, including disease and medication burden, patient behavior both intentional and unintentional, and cost-related burden associated with non-adherence. Higher Scores better the outcomes, measured within categories and overall adherence level.
Compare patients perceived Satisfaction of pharmaceutical care services
This will be assessed by using Nepali version of Patients Perceived satisfaction of Pharmacist care (PSPSQ. 2 ) questionnaire. This tool comprises 20 items questionnaire divided into three dimensions based on a four-point Likert scale. Dimensions include quality of care, pharmacist-patient relationships, and overall satisfaction. Higher scores represent better outcomes, measured within domains and overall satisfaction levels.
Change in Health related Quality of Life
Translated Nepali version of Euro 5 D 5 L questionnaire measures will be used to measure patients' health-related quality of life (HRQoL). This questionnaire created by the European Quality of Life Group (EuroQol Group) measure HRQoL in five dimension Mobility, Self-Care, Usual Activities, Pain/Discomfort, and Anxiety/Depression. Each dimension has five levels to describe the severity: no problem, slight problem, moderate problem, severe problem, and unable (very severe). The outcomes will be measured in the overall health utility index value. The index value ranges from -1 to 1 (0 indicates death, <0 indicates worse than death, and 1 indicates full health)

Secondary Outcome Measures

Change in routine clinical laboratory parameters of patients Lipid Profile test.
Data will be obtained from routine clinical laboratory test of patients blood Lipid Profile ( Total cholesterol, High density lipoprotein (HDL) Cholesterol, Low density lipoprotein (LDL) cholesterol, Very low density lipoprotein (VLDL) Cholesterol, and Triglycerides) measured in mg/dl.
Change in Patients health related Knowledge, Attitude and Practice
Patient knowledge, attitude and practice will be assessed using 25-item Disease related Health Knowledge, attitude and practice questionnaires developed by Investigators through literature review and content validated with a team of health care professionals. The higher the scores within domains better the outcomes.

Full Information

First Posted
January 6, 2023
Last Updated
August 22, 2023
Sponsor
Chettinad Academy of Research and Education (Deemed to be University)
Collaborators
Purbanchal University
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1. Study Identification

Unique Protocol Identification Number
NCT05707481
Brief Title
Impact of Clinical Pharmacist-Led Intervention on Management of Diabetic Hypertensive Patients in Eastern Nepal
Official Title
Impact of Clinical Pharmacist Led Intervention on Management of Diabetic Hypertensive Patients.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 22, 2023 (Actual)
Primary Completion Date
October 30, 2024 (Anticipated)
Study Completion Date
October 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chettinad Academy of Research and Education (Deemed to be University)
Collaborators
Purbanchal University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Diabetic-Hypertensives are at a higher risk of premature microvascular and macrovascular complications than diabetes alone. Proper lifestyle management, diet, disease monitoring, and medication adherence is essential in achieving desired therapeutic outcomes, preventing complications and improving those patients' Health-Related Quality of Life (HRQoL). Pharmacists are the most accessible healthcare professionals to the public and have a crucial role in optimizing treatment outcomes in patients with chronic diseases such as diabetes and hypertension. Experimental trials' demonstrating the potential roles of pharmaceutical services is scarce in the literature, particularly in developing countries of south Asia. Therefore, the investigators plan to conduct a prospective-interventional trial to determine the potential impacts of pharmacist-supervised educational intervention on the management of "Type II diabetic with comorbid hypertension" patients. Patient data will be collected using patient's clinical profile forms, General Medication adherence Scale (GMAS), Patients Satisfaction towards pharmaceutical services (PSPSQ), Health Related-KAP questionnaires. Data will be verified, stored, entered into databases, and analyzed according to the data management plan. The findings will be compared in terms of clinical and nonclinical outcome measures between the control and test groups to ascertain the conclusion.
Detailed Description
Diabetics are twice as likely as non-diabetics to develop hypertension. Hypertension is a strong predictor of adverse cerebulo-vascular and cardiovascular events in people with diabetes, which increases risk of Premature micro-vascular and macro-vascular problems in patients encompassing both diseases. Therefore, strict glycemic and blood pressure control is essential to subdue complication and prevent dreadful cardiovascular events such as stroke, Ischemia and myocardial infarction. Participants with both chronic diseases may have lower HRQoL due to increased susceptibility towards cardiovascular comorbidities. Adherence to medication is equally crucial for treatment success. Pharmacist in collaboration with other healthcare members, could play a vital role in the care of patients and optimizing treatment outcomes in patients with chronic diseases . Chronic disease management is of particular interest to clinical pharmacist since most intervention requires long-term prescription medication use. The international pharmaceutical federation (FIP) and world health organization (WHO) have implored pharmacists to support people with chronic disease through their expanded role that includes "pharmaceutical care." In Nepal, Clinical Pharmacy practice is still in early infancy, though few studies have shown encouraging impacts of pharmaceutical care services. Similarly, there is a significant gap in the literature in this region addressing the impact of pharmacist-supervised educational intervention on both clinical and nonclinical outcomes measures, primarily focusing on co-morbid Diabetes- Hypertensive patients. Therefore, these studies are intended to recap and fill that gap area and add new and valuable insight to the available literature.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes, Hypertension

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
92 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control group (Usual Standard Care)
Arm Type
No Intervention
Arm Description
Control group patient will undergo routine care by their physician and nurses. However, the investigator will only provide basic counseling regarding drug prescribed during discharge to the patients. In another term "Usual care" will be provided to the patients
Arm Title
Intervention Group (Clinical Pharmacist-led educational Intervention)
Arm Type
Other
Arm Description
In addition to routine care by physician and nurses, Patients in interventional group will receive two consecutive face to face interview and counseling of 20-40 minutes during the baseline period and the first follow-up period at 3-month by clinical pharmacist. Teaching and counseling session involves information on various non-pharmacological and pharmacological disease management strategies.
Intervention Type
Other
Intervention Name(s)
Clinical Pharmacist-Led Educational Intervention
Intervention Description
Non Pharmacological management strategies include information related to life style modification, healthy dietary habits, physical activity and stress management techniques. In contrast, pharmacological educational intervention involves disease -related information ( diabetes/hypertension sign and symptoms, risk factor, complications, self-monitoring of blood pressure/glucose, symptoms and management of hypoglycemia/hypotension etc. ) and drug related information ( prescribed drug name, indication, contraindication, adverse effects etc.) as well as importance of adherence to prescribed medication and strategies to minimize DRPs issues. These teaching sessions will be carried out with the help of verbal communication, audio visual demonstration (including charts,pictorial etc) and information leaflets. Furthermore, a copy of educational package would be given to each participant for reference and guidance.
Primary Outcome Measure Information:
Title
Change in blood pressure
Description
Assessed with measurement of Systolic and diastolic blood pressure in mmHg using sphygmomanometer
Time Frame
baseline, follow up at 3 months and 6 months respectively
Title
Change in blood glycemic profile
Description
Assessed with measurement of Fasting Blood Sugar (FBS) and Post Prandial Blood Sugar (PPBS) in mg/dl.
Time Frame
baseline, follow up at 3 months and 6 months respectively
Title
change in glycosylated hemoglobin (HbA1C) level
Description
assessed from patients glycosylated hemoglobin (HbA1C) level test, measured in percent (%)
Time Frame
baseline, follow up at 3 months and 6 months respectively
Title
Impact of Intervention in Patients Medication Adherence
Description
It will be measured using translated and validated Nepalese version of the 11-item Novel general medication adherence Scale (GMAS) questionnaire divided into three categories based on a four-level Likert scale. GMAS tools provide a wide range of components, including disease and medication burden, patient behavior both intentional and unintentional, and cost-related burden associated with non-adherence. Higher Scores better the outcomes, measured within categories and overall adherence level.
Time Frame
baseline, follow up at 3 months and 6 months respectively
Title
Compare patients perceived Satisfaction of pharmaceutical care services
Description
This will be assessed by using Nepali version of Patients Perceived satisfaction of Pharmacist care (PSPSQ. 2 ) questionnaire. This tool comprises 20 items questionnaire divided into three dimensions based on a four-point Likert scale. Dimensions include quality of care, pharmacist-patient relationships, and overall satisfaction. Higher scores represent better outcomes, measured within domains and overall satisfaction levels.
Time Frame
baseline, follow up at 3 months and 6 months respectively
Title
Change in Health related Quality of Life
Description
Translated Nepali version of Euro 5 D 5 L questionnaire measures will be used to measure patients' health-related quality of life (HRQoL). This questionnaire created by the European Quality of Life Group (EuroQol Group) measure HRQoL in five dimension Mobility, Self-Care, Usual Activities, Pain/Discomfort, and Anxiety/Depression. Each dimension has five levels to describe the severity: no problem, slight problem, moderate problem, severe problem, and unable (very severe). The outcomes will be measured in the overall health utility index value. The index value ranges from -1 to 1 (0 indicates death, <0 indicates worse than death, and 1 indicates full health)
Time Frame
baseline, follow up at 3 months and 6 months respectively
Secondary Outcome Measure Information:
Title
Change in routine clinical laboratory parameters of patients Lipid Profile test.
Description
Data will be obtained from routine clinical laboratory test of patients blood Lipid Profile ( Total cholesterol, High density lipoprotein (HDL) Cholesterol, Low density lipoprotein (LDL) cholesterol, Very low density lipoprotein (VLDL) Cholesterol, and Triglycerides) measured in mg/dl.
Time Frame
baseline, follow up at 3 months and 6 months respectively
Title
Change in Patients health related Knowledge, Attitude and Practice
Description
Patient knowledge, attitude and practice will be assessed using 25-item Disease related Health Knowledge, attitude and practice questionnaires developed by Investigators through literature review and content validated with a team of health care professionals. The higher the scores within domains better the outcomes.
Time Frame
baseline, follow up at 3 months and 6 months respectively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
68 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male and female patients aged 40 to 68 years. Clinically diagnosed with type II diabetes mellitus with hypertension as co-morbidity. Minimum one year of the medical history of diabetic and hypertension. Minimum 6 months on antidiabetic as well as antihypertensive medication therapy. Patients willing to participate in the study and those providing written informed consent for participation. Exclusion Criteria: Patients with Type I diabetes mellitus, Diabetic insipidus, Gestational diabetes or other forms of diabetes. Presence of other chronic disease co-morbidity other than hypertension and diabetes complications. Mentally incompetent patients, Pregnant, critically ill patients (requiring hospital admission). Patients have tuberculosis, Corona virus, and other highly communicable diseases. Those patients not willing to performing routine follow-up visit.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Prasanna Dahal, PharmD
Phone
+9779819316086
Email
drprasannadahal@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Prasanna Dahal, PharmD
Organizational Affiliation
Chettinad Academy of Research and Education (Deemed to be University)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Purbanchal University Hospital
City
Gothgaun,Sundar Haraicha Municipality, Morang
State/Province
Province 1
ZIP/Postal Code
56600
Country
Nepal
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Prasanna Dahal, PharmD
Phone
+9779819316086
Email
drprasannadahal@gmail.com
First Name & Middle Initial & Last Name & Degree
Deevan Paul A, PhD
First Name & Middle Initial & Last Name & Degree
Kadir Alam, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30863660
Citation
Naqvi AA, Hassali MA, Jahangir A, Nadir MN, Kachela B. Translation and validation of the English version of the general medication adherence scale (GMAS) in patients with chronic illnesses. J Drug Assess. 2019 Feb 6;8(1):36-42. doi: 10.1080/21556660.2019.1579729. eCollection 2019.
Results Reference
background
PubMed Identifier
34475753
Citation
Shrestha R, Sapkota B, Khatiwada AP, Shrestha S, Khanal S, Kc B, Paudyal V. Translation, Cultural Adaptation and Validation of General Medication Adherence Scale (GMAS) into the Nepalese Language. Patient Prefer Adherence. 2021 Aug 27;15:1873-1885. doi: 10.2147/PPA.S320866. eCollection 2021.
Results Reference
background
PubMed Identifier
25481330
Citation
Sakharkar P, Bounthavong M, Hirsch JD, Morello CM, Chen TC, Law AV. Development and validation of PSPSQ 2.0 measuring patient satisfaction with pharmacist services. Res Social Adm Pharm. 2015 Jul-Aug;11(4):487-98. doi: 10.1016/j.sapharm.2014.10.006. Epub 2014 Oct 22.
Results Reference
background
PubMed Identifier
33035243
Citation
Shrestha S, Sapkota B, Thapa S, K C B, Khanal S. Translation, cross-cultural adaptation and validation of Patient Satisfaction with Pharmacist Services Questionnaire (PSPSQ 2.0) into the Nepalese version in a community settings. PLoS One. 2020 Oct 9;15(10):e0240488. doi: 10.1371/journal.pone.0240488. eCollection 2020.
Results Reference
background
Links:
URL
https://euroqol.org/eq-5d-instruments/eq-5d-5l-about/
Description
The 5-level EQ-5D version (EQ-5D-5L) was introduced by the EuroQol Group in 2009 to improve the instrument's sensitivity and to reduce ceiling effects, as compared to the EQ-5D-3L.

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Impact of Clinical Pharmacist-Led Intervention on Management of Diabetic Hypertensive Patients in Eastern Nepal

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