NCT07757399Not yet recruiting
The Therapeutic Effects of Ceylon Cinnamon Supplementation and a Self-Efficacy Educational Program on Glycemic Control, Lipid Profiles, and Pain in Type 2 Diabetes Mellitus With Painful Diabetic Peripheral Neuropathy
The Therapeutic Effects of Ceylon Cinnamon Supplementation and a Self-Efficacy Educational Program on Glycemic Control, Lipid Profiles, and Pain in Type 2 Diabetes Mellitus With Painful Diabetic Peripheral Neuropathy: A Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 11 Aug 2026
Brief summary (registry, in English)
This randomized controlled trial aims to evaluate the therapeutic effects of pure Ceylon cinnamon (Cinnamomum verum) supplementation combined with a structured self-efficacy-based educational program on glycemic control, lipid profiles, and neuropathic pain in adult patients with type 2 diabetes mellitus (T2DM) and painful diabetic peripheral neuropathy (PDPN). A total of 900 participants will be randomly assigned to three parallel arms: a standard care control group, a Ceylon cinnamon supplementation group (1,000 mg/day), and a combined intervention group (Ceylon cinnamon supplementation plus the self-efficacy educational program) over a 6-month period. The study hypothesizes that the combined approach will significantly improve glycemic parameters, reduce neuropathic pain severity, and enhance metabolic profiles compared to standard care alone.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 900 (estimated)
- First submitted
- 31 Jul 2026
- Start date
- 1 Aug 2026
- Primary completion date
- 1 Dec 2026
- Lead sponsor
- Jerash Private University
- Diseases
- Type 2 diabetes
- NCT number
- NCT07757399
What you commit to
- Study type: Interventional
- Planned participants: 900
- From 1 Aug 2026 to the primary completion date, 1 Dec 2026
- No sites listed in no 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.
Prior treatment
- Concurrent participation in another clinical trial or severe psychiatric/cognitive disorders that hinder study participation.
Other illness
- Type 1 diabetes mellitus or gestational diabetes.
- Severe renal or hepatic impairment.
- Known allergy, hypersensitivity, or contraindication to cinnamon or related botanical products.
Other
- Pregnancy or lactation.
Who the study is looking for
- Diagnosed with Type 2 Diabetes Mellitus (T2DM) for at least 6 months.
- Confirmed diagnosis of painful diabetic peripheral neuropathy (PDPN).
- Age between 18 and 65 years.
- Able to provide written informed consent and willing to comply with the study protocol, supplement intake, and educational sessions.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.