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NCT07863934Completed

Effects of High-Intensity Interval Training and Quinoa Supplementation in Women With Type 2 Diabetes

Effects of High-Intensity Interval Training and Quinoa Supplementation on Some Selected Pyroptosis Proteins and Glycemic Control in Women With Type 2 Diabetes: A Randomized Controlled Trial.

Source: ClinicalTrials.gov · Last updated 7 Oct 2026

Brief summary (registry, in English)

This study evaluated the effects of eight weeks of high-intensity interval training (HIIT), daily quinoa consumption, and their combination on inflammatory markers and blood glucose control in women aged 50-65 years with type 2 diabetes. Participants were randomly assigned to four groups: HIIT, quinoa consumption, combined HIIT and quinoa consumption, or control. The quinoa groups consumed 25 g of cooked quinoa daily for eight weeks. Blood markers and body measurements were assessed before and after the intervention.

Status (registry)
Completed
Study type
Interventional
Enrollment
32 (actual)
First submitted
2 Oct 2026
Start date
16 Oct 2024
Primary completion date
28 Dec 2024
Lead sponsor
University of Central Lancashire
NCT number
NCT07863934

What you commit to

  • Study type: Interventional
  • Participants enrolled: 32
  • From 16 Oct 2024 to the primary completion date, 28 Dec 2024
  • 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.

Prior treatment

  • Current insulin therapy

Other illness

  • Diagnosed cardiovascular disease
  • Thyroid disorders

Other

  • Diabetic foot ulcers
  • Recent hospitalization
  • Regular participation in a structured exercise programme
  • Exercise intolerance, specifically manifested by: discomfort, severe fatigue, imbalance or dizziness

Who the study is looking for

  • Female
  • 50-65 years of age
  • Diagnosed with type 2 diabetes for at least 5 years
  • Fasting blood glucose \>126 mg/dL OR HbA1c ≥6.5%
  • Receiving metformin therapy
  • Able to participate safely in the exercise intervention
  • Able and willing to provide written informed consent

Age in the registry: 50 years to 65 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Allameh Tabataba'i University
Coordinator of this site? Confirm its status
TehranIranUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.