Effectiveness of Education, Medication Adjustment and Telemonitoring in Reducing Diabetes Complications During Ramadan

Sponsor
Sengkang General Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT06033872
Collaborator
SingHealth Polyclinics (Other), Singapore Clinical Research Institute (Other)
79
1
2
16.1
4.9

Study Details

Study Description

Brief Summary

Introduction Diabetes is a global emergency with detrimental clinical and financial consequences. Poorly managed diabetes leads to a myriad of serious complications, especially cardiovascular and infectious complications, with consequent increased cost and mortality rate. For Muslims in particular, the annual fasting month of Ramadan is one such period when diabetes control is essential. Adequate adjustments in diabetes management need to be made in line with the allowed meal times to avoid the risk of diabetes complications during Ramadan.

Objective Investigators aim to investigate the effectiveness of focused diabetes education and medication adjustment with telemonitoring to reduce diabetes complications during Ramadan fasting as well as to assess the cost-effectiveness of this intervention for Muslims with diabetes in Singapore.

Methodology In a parallel group randomized controlled trial, investigators aim to recruit 100 adults with diabetes who are able to fast at least 15 days in Ramadan. You will be randomized to the intervention group comprising of focused diabetes education, medication adjustment and telemonitoring, and control group receiving standard care. You will be followed up during Ramadan. The primary outcome is the incidence of hypoglycemia in Ramadan. The secondary outcomes are (i) incidence of other diabetes complications in Ramadan episodes including hyperglycemia, episodes of acute infections, attendances in clinic and emergency department and that of hospital admission, and (ii) cost-effectiveness of the intervention.

Clinical Significance The study enables investigators to evaluate focused pre-Ramadan diabetes education and medication adjustment with tele-monitoring as a means to reduce the markedly increased risk of diabetes complications for a large population during the fasting month, with potential for increased cost-effectiveness through reducing unscheduled attendances at clinic and hospital.

Condition or Disease Intervention/Treatment Phase
  • Combination Product: Focused education, medication adjustment and telemonitoring
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
79 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effectiveness of Diabetes Education and Medication Adjustment With Telemonitoring Intervention in Reducing Diabetes Complications During Ramadan Fasting - a Randomized Control Trial
Actual Study Start Date :
Jan 25, 2021
Actual Primary Completion Date :
Sep 1, 2021
Actual Study Completion Date :
May 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Intervention

Focused education, medication adjustment and telemonitoring

Combination Product: Focused education, medication adjustment and telemonitoring
Focused diabetes education session for Ramadan fasting You will be taught to record Meal plans Physical activities Blood glucose monitoring, and Monitoring for diabetes complications. Then perform a trial fasting day prior to Ramadan when control is not optimal or medication with risk of hypoglycemia. Medication adjustment for Ramadan fasting You will be provided regimen modified for Ramadan fasting. Telemonitoring You will be taught to perform blood glucose monitoring 4 times daily using a glucometer and upload recordings of glucose levels onto the data software.

No Intervention: Control

Standard care

Outcome Measures

Primary Outcome Measures

  1. a. To compare the first incidence rate of hypoglycemia or severe hypoglycemia between intervention and control groups in Ramadan [30 day]

Secondary Outcome Measures

  1. i. To compare the first incidence rate of hypoglycemia or severe hypoglycemia between intervention and control groups in Ramadan when compared to before and after Ramadan [12 weeks]

  2. ii. To compare the first incidence rate of complications in Ramadan when compared to before and after 1. Hyperglycemia and crises 2. Acute infections, clinic and emergency department attendances and hospital admissions [12 weeks]

  3. Health-related Quality-of-Life using European Quality of Life Five Dimensions (EQ-5D) - to provide a summary of index value of health and health change, cost-utility calculation. [17 weeks]

    Five dimensions are mobility, self-care, usual activities, pain or discomfort and anxiety or depression. Scored health as 0 to 100 where 0 is worst and 100 is best

  4. Healthcare utilizations costs - Medical services, drugs and devices utilized, outpatient and inpatient visits, cost of intervention sessions, telemonitoring and equipment, indirect costs related to health care utilisation, and caregiver costs. [17 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
You must meet all of the inclusion criteria to participate in this study:
  1. Adults aged at least 21 years old,

  2. Able to fast at least 15 days in Ramadan based on experience of fasting in previous year's Ramadan,

  3. Known physician-diagnosed diabetes mellitus (DM) based on the following criteria before starting treatment

  1. Symptoms of polyuria, polydipsia and unexplained weight loss with i. fasting glucose ≥ 7.0mmol/l or ii. random plasma glucose ≥ 11.1 mmol/l or iii. 2-hour post 75g oral glucose challenge test plasma glucose ≥ 11.1 mmol/l b. Absence of symptoms of polyuria, polydipsia and unexplained weight loss with the following tests done twice showing the values i. fasting glucose ≥ 7.0mmol/l or ii. random plasma glucose ≥ 11.1 mmol/l or iii. 2-hour post 75g oral glucose challenge test plasma glucose ≥ 11.1 mmol/l
  1. Performed laboratory tests as per standard care : serum glycated hemoglobin A1c (HbA1c) level, blood Low Density Lipoprotein-Cholesterol, blood triglyceride level, blood High Density Lipoprotein-Cholesterol, blood Total Cholesterol and serum creatinine

  2. Most recent HbA1c level was >7.0% (>53mmol/mol)

  3. Ability to give informed consent,

  4. Ability to perform weekly recordings in the diary,

  5. Able to use and owns a mobile phone for recordings on mobile application

  6. Should have had DM-related clinic visits or hospitalization in the past 10 months.

Exclusion Criteria:
Meeting any of the exclusion criteria at baseline will exclude you from participation:
  1. Severe diabetes complications including end-stage renal failure, severe hypoglycemia and hyperglycemic crises within the last 1 month negating ability to fast,

  2. Pregnancy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sengkang General Hospital Singapore Singapore

Sponsors and Collaborators

  • Sengkang General Hospital
  • SingHealth Polyclinics
  • Singapore Clinical Research Institute

Investigators

  • Principal Investigator: Sueziani B Zainudin, MBBS FRCPG, Sengkang General Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sengkang General Hospital
ClinicalTrials.gov Identifier:
NCT06033872
Other Study ID Numbers:
  • 2019/2888
First Posted:
Sep 13, 2023
Last Update Posted:
Sep 14, 2023
Last Verified:
Sep 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 14, 2023