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A Clinical Guideline-based Management of Type-2 Diabetes by Ayurvedic Practitioners in Nepal

Primary Purpose

Diabetes, Type2Diabetes, Diabetes Mellitus

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Clinical Guideline based Management
Comparator
Sponsored by
Nepal Health Research Council
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes focused on measuring Ayurveda, DiabetesMellitus, ClinicalGuideline

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • aged ≥18 years
  • new T2DM patients (i.e., treatment naïve), diagnosed by the participating Ayurvedic practitioner
  • able to provide written informed consent.

Exclusion Criteria:

  • Pregnant women
  • those with any serious or uncontrolled medical condition (e.g., cancer)
  • those currently receiving (or has plans to receive during the study period) any related non-pharmaceutical/pharmaceutical intervention.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Intervention

    Comparator

    Arm Description

    Clinical guideline-based management of T2DM by Ayurvedic practitioners. The clinical guideline will cover topics like diagnostic criteria, blood glucose targets, lifestyle advice, Ayurvedic medicines, monitoring and follow-up (including screening for complications and referral to specialists for complications management). The clinical guideline will make recommendations based on the best available evidence. Ayurvedic practitioners will have at least a 5½ year undergraduate medical degree in Ayurveda. Regular training will be provided to Ayurvedic practitioners (in groups) in the use of clinical guideline which will involve roleplaying and structured and instructive feedback to improve their performance. The trainings will be recorded on the Training Attendance Log and they will be provided a Training Certificate for completing the training.

    Comparator: Currently, no standard clinical guideline is used by Ayurvedic practitioners to manage T2DM in Nepal. Thus, the comparator will be the usual management of T2DM (i.e., without any clinical guideline) by Ayurvedic practitioners. Participants will continue their medications for other systemic diseases, if any.

    Outcomes

    Primary Outcome Measures

    To assess the change in the management of type-2 Diabetes with the introduction of Clinical Guideline
    The assessment will be done in the baseline and the end line by measuring HbA1C
    To assess the change Health related quality of life with the introduction of clinical guideline
    Health related quality of life will be assessed in the baseline and the end line through HRQOL questionnaire

    Secondary Outcome Measures

    To determine the rate of dropout
    To compare the rate of dropout in the intervention and control group ,
    To determine the number of participants who adhere to the guideline
    To determine the rate of participants adhering to the guideline

    Full Information

    First Posted
    February 8, 2022
    Last Updated
    May 17, 2022
    Sponsor
    Nepal Health Research Council
    Collaborators
    University of Nottingham
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05259735
    Brief Title
    A Clinical Guideline-based Management of Type-2 Diabetes by Ayurvedic Practitioners in Nepal
    Official Title
    A Clinical Guideline-based Management of Type-2 Diabetes by Ayurvedic Practitioners in Nepal: a Feasibility Cluster Randomised Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    May 2022 (Anticipated)
    Primary Completion Date
    March 2023 (Anticipated)
    Study Completion Date
    March 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Nepal Health Research Council
    Collaborators
    University of Nottingham

    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
    T2DM is a complex disorder which has major health, social and economic consequences. Its chronic hyperglycaemia is associated with macro- and micro-vascular complications and even death. The prevalence of T2DM in Nepal is high. In Nepal, Ayurveda is the dominant traditional medical system and is in use for thousands of years, especially for meeting the primary healthcare needs. Lack of availability of western medical system doctors in rural areas is another reason. In recognition of these facts, the Nepalese government actively promotes Ayurveda and deploys Ayurvedic practitioners in PHCs, often as the main clinical provider. This is a two-arm, feasibility cluster RCT with blinded outcome assessment and integrated qualitative process evaluation will be conducted in 12 Ayurvedic Primary Health Care Center Participants who are aged 18 years or above, new T2DM patients (i.e., treatment naïve), diagnosed by the participating Ayurvedic practitioner and able to provide written informed consent will be enrolled in the study. Each participant will be involved in the study for six months. Patient will be assessed for Glycated haemoglobin, Lipid Profile, Physiological parameters like heart rate and pulse rate, Anthropometric parameters, EuroQol-5D-5L
    Detailed Description
    In Nepal, Ayurveda is the dominant traditional medical system and is in use for thousands of years, especially for meeting the primary healthcare needs. The classical texts are written in Sanskrit, an ancient language. T2DM is one of the top diseases for which patients consult Ayurvedic practitioners, and many T2DM patients use Ayurvedic treatments, often from the beginning and exclusively and throughout their lives.Ayurveda fits their health beliefs and culture. Acceptability, satisfaction and perceived relief are usually high, especially among rural, poor, older and tribal populations. Many T2DM patients prefer not to use western medicines - to avoid the associated side-effects and costs and the mode of administration like insulin injections. Lack of availability of western medical system doctors in rural areas is another reason. In recognition of these facts, the Nepalese government actively promotes Ayurveda and deploys Ayurvedic practitioners in PHCs, often as the main clinical provider. Strong concerns remain about the sub-optimal T2DM management of many patients, arising from the unacceptable variations in Ayurvedic clinical practice. The actions to be taken at different stages of the T2DM care pathway are largely left to the judgment of the individual Ayurvedic practitioner (including screening for complications and referral to specialists), resulting in these unacceptable variations. Despite the clinical effectiveness and safety of several Ayurvedic medicines for managing T2DM found in trial settings, many non-evidence based herbal and herbo-mineral medicines are prescribed by them in real practice, which can have serious adverse effects on patients, including heavy metal poisoning. It is exceedingly difficult for them to be versed with the latest data on most effective and safe Ayurvedic medicines. One of the major challenges identified by them in their clinical decision-making process and delivering quality care to T2DM patients is the absence of a good quality clinical guideline. Its absence forces many of them to blindly follow the claims made by others or use a 'trial and error' approach. Faced with similar issues in the western medical system, clinical guidelines have been effectively deployed in every aspect of clinical care in the last few decades. For example, clinical trials conducted in English and Mexican primary care settings found that the introduction of clinical guidelines was effective in managing T2DM. Despite their pervasive use in the western medical system, their existence in Ayurvedic clinical practice remains extremely limited. Many stakeholders, including Ayurvedic practitioners, patient groups, the Nepalese government and WHO, are advocating for good quality clinical guidelines for Ayurvedic practitioners. Thus, a good quality clinical guideline, based on the best available evidence, to manage T2DM by Ayurvedic practitioners may address the problems mentioned above. We searched a range of trial registries and databases, and no study is investigating the utility of such an intervention for managing T2DM by Ayurvedic practitioners. Thus, there is a need for a robustly designed pragmatic study to evaluate such an innovative approach. This is a two-arm, feasibility cluster RCT with blinded outcome assessment and integrated qualitative process evaluation. 12 Primary Health Centres (PHCs) with at least one Ayurvedic practitioner (most have only one) for the duration of the study and willing to participate in the study will be randomised (1:1) to intervention or comparator groups by an independent statistician according to a computer-generated randomisation schedule. PHCs should be screened for eligibility (PHC Screening and Randomisation Form) and recorded on the Screening of PHCs Eligible PHCs will be randomised and provided Site ID. Ayurvedic practitioners and patients cannot be 'blinded' to group allocation, but the outcome assessor will be 'blind'.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Diabetes, Type2Diabetes, Diabetes Mellitus
    Keywords
    Ayurveda, DiabetesMellitus, ClinicalGuideline

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Masking Description
    Final outcome assessment will be conducted after 6 month for both arms by blind assessor.
    Allocation
    Randomized
    Enrollment
    120 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Intervention
    Arm Type
    Experimental
    Arm Description
    Clinical guideline-based management of T2DM by Ayurvedic practitioners. The clinical guideline will cover topics like diagnostic criteria, blood glucose targets, lifestyle advice, Ayurvedic medicines, monitoring and follow-up (including screening for complications and referral to specialists for complications management). The clinical guideline will make recommendations based on the best available evidence. Ayurvedic practitioners will have at least a 5½ year undergraduate medical degree in Ayurveda. Regular training will be provided to Ayurvedic practitioners (in groups) in the use of clinical guideline which will involve roleplaying and structured and instructive feedback to improve their performance. The trainings will be recorded on the Training Attendance Log and they will be provided a Training Certificate for completing the training.
    Arm Title
    Comparator
    Arm Type
    Active Comparator
    Arm Description
    Comparator: Currently, no standard clinical guideline is used by Ayurvedic practitioners to manage T2DM in Nepal. Thus, the comparator will be the usual management of T2DM (i.e., without any clinical guideline) by Ayurvedic practitioners. Participants will continue their medications for other systemic diseases, if any.
    Intervention Type
    Combination Product
    Intervention Name(s)
    Clinical Guideline based Management
    Intervention Description
    Clinical guidline based management will be done for Type 2 diabetes Mellitus
    Intervention Type
    Other
    Intervention Name(s)
    Comparator
    Intervention Description
    In this arm usual management of T2DM without any clinical guideline
    Primary Outcome Measure Information:
    Title
    To assess the change in the management of type-2 Diabetes with the introduction of Clinical Guideline
    Description
    The assessment will be done in the baseline and the end line by measuring HbA1C
    Time Frame
    Assessment will be done from the data of screening until the 6 months
    Title
    To assess the change Health related quality of life with the introduction of clinical guideline
    Description
    Health related quality of life will be assessed in the baseline and the end line through HRQOL questionnaire
    Time Frame
    Assessment will be done from the data of screening until the 6 months
    Secondary Outcome Measure Information:
    Title
    To determine the rate of dropout
    Description
    To compare the rate of dropout in the intervention and control group ,
    Time Frame
    From the date of screening until the 6 months
    Title
    To determine the number of participants who adhere to the guideline
    Description
    To determine the rate of participants adhering to the guideline
    Time Frame
    From the date of screening until the 6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: aged ≥18 years new T2DM patients (i.e., treatment naïve), diagnosed by the participating Ayurvedic practitioner able to provide written informed consent. Exclusion Criteria: Pregnant women those with any serious or uncontrolled medical condition (e.g., cancer) those currently receiving (or has plans to receive during the study period) any related non-pharmaceutical/pharmaceutical intervention.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Meghnath Dhimal, PhD
    Phone
    9851167198
    Email
    meghdhimal2@gmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Bihumgum Bista, MPH
    Phone
    9845537861
    Email
    bistabihungum@gmail.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Kaushik Chattopadhyay, MPH
    Organizational Affiliation
    University of Nottingham
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Pradip Gyanwali, MD
    Organizational Affiliation
    Nepal Health Research Council
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    A Clinical Guideline-based Management of Type-2 Diabetes by Ayurvedic Practitioners in Nepal

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