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Comparison of two exercise- therapy programs on indices of muscular strength in female type 2 diabetes mellitus patients.

Comparison of two exercise- therapy programs on indices of muscular strength in female type 2 diabetes mellitus patients: a double blind randomized controlled trial.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201104256283N1
Enrollment
40
Registered
2011-12-27
Start date
2011-05-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Exercise therapy programs in Non-insulin-dependent diabetes mellitus type II. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: Supervised exercise protocol (SEP). Intervention 2: Home-based exercise protocol (HEP).
Supervised exercise protocol (SEP)
Home-based exercise protocol (HEP)

Sponsors

Vice Chancellor for research of Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Type 2 diabetes mellitus; Age range: 30-55 years; Female; Treated by Oral Anti Diabetic agents; HbA1C=8-10%. Exclusion criteria: High blood pressure; Insulin therapy; B-Blocker agents; Ca- Channel blockers; Nitrates; Cardio Vascular Diseases; Micro vascular and Macro vascular side effects of Diabetes Mellitus; History of moderate to sever muscoloskeletal disorders;Anemia (Hb lower than12); Pregnancy;Tobacco smoking; Alcohol abuse.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Strenght changes of concentric and eccentric muscles. Timepoint: 72-96 hours before the initiation of the protocols , 72-96 hours after the conclusion of the protocols. Method of measurement: Isokinetic test by Kin Kam device.

Secondary

MeasureTime frame
Eccentric average torque of non-dominant knee extensors. Timepoint: 72-96 hours before the initiation of the protocols , 72-96 hours after the conclusion of the protocols. Method of measurement: Isokinetic test.;Maximal concentric angular velocity of non-dominant knee extensors. Timepoint: 72-96 hours before the initiation of the protocols , 72-96 hours after the conclusion of the protocols. Method of measurement: Isokinetic test.;Eccentric peak torque of non-dominant knee extensors. Timepoint: 72-96 hours before the initiation of the protocols , 72-96 hours after the conclusion of the protocols. Method of measurement: Isokinetic test.;Concentric avereage torque of non-dominant knee extensors. Timepoint: 72-96 hours before the initiation of the protocols , 72-96 hours after the conclusion of the protocols. Method of measurement: Isokinetic test.;Maximal eccentric angular velocity of non-dominant knee extensors. Timepoint: 72-96 hours before the initiation of the protocols , 72-96 hours after the conclusion of the protocols. Method of measurement: Isokinetic test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Laily Najafi

Endocrine research center (Firozgar), Tehran University of Medical Sciences

l.najafi@yahoo.com+98 21 8894 5247

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026