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Muscle Soreness and Protective Effect of Oestroge

Not Applicable
Conditions
Muscle soreness.
Pain in limb
Registration Number
IRCT138903284203N1
Lead Sponsor
Vice-Chancellor for research, Semnan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
24
Inclusion Criteria

1- aged between 18-25years, 2- giving written consent
Exclusion criteria: 1- Neuro-muscular disease, 2- Cardiovascular disease, 3- Diabetes mellitus, 4- Renal failure, 5- Acute herniation, 6- Discopathy, 7- High blood pressure, 8- Asthma and respiratory problems, 9- Acute infection, 10- Recent fracture in skeletal system, 11- Pin, plaques and other fixations in lower limbs, 12- Total hip arthroplasty, 13- Total knee arthroplasty, 14- Cardiac pacemaker, 15- Pregnancy, 16- Previous history of muscular injection a week before intervention, 17- Previous history of participation in body building program, 18- Previous history of participation in aerobic program, 19- unfinished trial sessions, 20- any reluctances to continue and willing to quit the study

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Creatine kinase enzyme of serum. Timepoint: Before intervention, 24 and 48 hours after intervention. Method of measurement: Blood sample.
Secondary Outcome Measures
NameTimeMethod
Maximal voluntary isometric strength of quadriceps muscle. Timepoint: before intervention, 24 and 48 hours after intervention. Method of measurement: With Loadcell, in 100 degrees flexion of knee.;Perceived pain. Timepoint: Before intervention, 24 and 48 hours after intervention. Method of measurement: A 10-mm Visual Analogue Scale (VAS).;Pressure pain threshold. Timepoint: Before intervention, 24 and 48 hours after intervention. Method of measurement: A 20 ml syringe with a spring inside, rounded tip.;Thigh circumference. Timepoint: Before intervention, 24 and 48 hours after intervention. Method of measurement: A tape measure, at 5, 10 and 15 cm above patella.
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