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The effect of 8 weeks of exercise on some diabetes-related factors in women with type 2 diabetes

The Effect of Eight Weeks of Exercise Snacks on Glycemic and Inflammatory Markers in Individuals with Type 2 Diabetes

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191123045478N3
Enrollment
45
Registered
2026-04-18
Start date
2026-04-21
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 diabetes mellitus (T2DM). Type 2 diabetes mellitus

Interventions

Intervention 1: Intervention group: Exercise snack group: Eight weeks of full-body resistance training consisting of 15 exercises:biceps curl with dumbbell,leg extension,sit-up,triceps extension with

Sponsors

Alzahra University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Having a definitive diagnosis of type 2 diabetes Having type 2 diabetes for more than a year Having cardiovascular, kidney, and eye diseases, diabetic foot ulcers, and nephropathy Ability to perform sports movements Absence of other severe chronic diseases such as thyroid, cardiovascular diseases, rheumatism, high blood pressure, Not participating in a sports program in the past six months

Exclusion criteria

Exclusion criteria: Pregnancy advanced cardiovascular disease movement problems that prevent exercise Participate in regular exercise programs before studying. Use of hormonal drugs Unwillingness to continue participating in the research long-term absences, and more than 2 to 3 sessions in training Inability of individuals to continue exercising for reasons such as severe hypoglycemia during exercise Menopause

Design outcomes

Primary

MeasureTime frame
Fasting blood glucose. Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Blood test.;Glycated hemoglobin (HbA1c). Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Blood test.;Fructosamine. Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Blood test.;Glycated albumin. Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Blood test.;Homeostatic Model Assessment for Insulin Resistance (HOMA-IR). Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Blood test.;High-sensitivity C-reactive protein (hs-CRP). Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Blood test.;Growth Differentiation Factor 15 (GDF15). Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Blood sampling performed using ELISA kits.;Lipid profile. Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Blood test.;Blood pressure. Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Using a mercury sphygmomanometer

Secondary

MeasureTime frame
Diabetes-related quality of life. Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Diabetes-Related Quality of Life Questionnaire.;Fatigue. Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Multidimensional Fatigue Questionnaire.;Sleep quality. Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Pittsburgh Sleep Quality Index.;Muscle strength. Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Handgrip dynamometer.;Timed Up and Go (TUG). Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (48 hours after the last training session). Method of measurement: Using the Timed Up and Go (TUG) test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Shakoor

Alzahra University

eli-shakoor@yahoo.com+98 21 8569 2669

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026