NCT07793292Not yet recruiting
Telehealth Educational Intervention for Adults With Type 2 Diabetes in Oman
Effectiveness of a Telehealth Educational Intervention on Glycemic Control, Medication Adherence, and Quality of Life Among Adults With Type 2 Diabetes in Oman: Study Protocol for a Two-Arm Parallel Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 28 Aug 2026
Brief summary (registry, in English)
The goal of this clinical trial is to find out whether adding a nurse-led telehealth educational program to usual diabetes care can improve blood sugar control, medication-related behaviors, and quality of life in adults with type 2 diabetes in Oman. The main question this study aims to answer is whether adults who receive the telehealth educational program, in addition to their usual diabetes care, have better blood sugar control after 6 months than adults who receive usual diabetes care alone. Blood sugar control will be assessed using hemoglobin A1c (HbA1c), a blood test that reflects average blood sugar levels over the previous few months. The study will also examine whether the telehealth program improves participants' attitudes and behaviors related to taking their diabetes medicines and their diabetes-related quality of life. Among participants receiving the telehealth intervention, the study will also assess how easy, useful, reliable, and satisfactory they find the telehealth service. Approximately 160 Omani adults with type 2 diabetes will take part in the study. Participants will be randomly assigned to one of two groups. One group will continue usual diabetes care and will also receive an individual telehealth education session once a week for 24 weeks. Each session will last about 20 to 30 minutes and will be provided by a trained nurse using an approved secure telehealth platform. The sessions will cover topics such as diabetes and HbA1c, safe use of medicines, strategies for remembering medicines, healthy eating, physical activity, blood glucose monitoring, recognition of low and high blood sugar, prevention of diabetes complications, stress and sleep, and communication with healthcare professionals. The other group will continue to receive usual diabetes care without the additional study telehealth education program. No established diabetes care will be withheld from either group, and the telehealth education will not replace routine medical care or authorize the research team to change participants' medications. Participants will be assessed at the start of the study, at 3 months, and at 6 months. Assessments will include HbA1c testing and questionnaires about medication-related beliefs and behaviors and diabetes-related quality of life. Participants in the telehealth group will also complete a questionnaire about their experience with and satisfaction with telehealth.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 160 (estimated)
- First submitted
- 25 Aug 2026
- Start date
- 1 Nov 2026
- Primary completion date
- 30 Nov 2027
- Lead sponsor
- Sultan Qaboos University
- Diseases
- Type 2 diabetes
- NCT number
- NCT07793292
What you commit to
- Study type: Interventional
- Planned participants: 160
- From 1 Nov 2026 to the primary completion date, 30 Nov 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Type 1 diabetes, gestational diabetes, or another diabetes type for which the intervention and outcome plan is not appropriate.
- Severe cognitive impairment, active psychosis, or another condition preventing informed consent or meaningful participation.
Other
- Current pregnancy or planned pregnancy during follow-up.
- Acute medical instability or hospital admission at recruitment.
- Participation in another interventional study that could materially affect trial outcomes.
- Inability to use telehealth even with reasonable assistance or absence of a private and safe setting for sessions.
- Another clinical or ethical reason identified by the treating clinician or principal investigator that makes participation inappropriate.
Who the study is looking for
- Participants must meet all of the following:
- Omani national aged 18 years or older.
- Confirmed type 2 diabetes mellitus (T2DM) documented in the medical record.
- Prescribed at least one glucose-lowering medication and receiving treatment for at least 3 months before enrollment.
- Most recent clinically valid HbA1c, or screening HbA1c when appropriate, 7.5% or higher.
- Access to an internet-enabled smartphone, tablet, or computer and ability to participate in video- or audio-supported telehealth sessions.
- Able to understand Arabic or English sufficiently to provide informed consent and participate in study procedures, and able to complete the validated Arabic Oman version of the medication-adherence questionnaire.
- Willingness to be randomized and availability for 6 months of follow-up.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Sultan Qaboos University Hospital Coordinator of this site? Confirm its status | Muscat | Oman | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.