postpolio syndrome. Postpolio syndrome
Conditions
Interventions
Intervention 1: The control group will receive no intervention and positive results, after the completion of research, will also be provided to the control group. Intervention 2: The first interventio
Rehabilitation
The control group will receive no intervention and positive results, after the completion of research, will also be provided to the control group.
The first intervention group will receive resistance training without restricted blood flow. Exercises will be started with a speed of 2 km/h for 3 minutes on a stationary bike with low resistance to
The second intervention group will receive resistance training with restricted blood flow. Exercises will be started with a speed of 2 km/h for 3 minutes on a stationary bike with low resistance to w
Sponsors
Vice chancellor of research, Tabriz University of Medical Science
Eligibility
Sex/Gender
Male
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria Men with the known syndrome as post-polio with records in the disabled community in Tabriz; Ages between 20 to 60 years; The ability to walk at least at home, with or without assistive devices; The ability to pedal a stationary bicycle loaded with at least 25 watts; Life expectancy at least more than a year Exclusion criteria The use of psychotropic drugs or other forms of psychotherapy; Depressive men according to the Beck depression (more than 6); Having other comorbidities, according to medical examination and information in the medical records that limit interventional programs such as cardiovascular diseases, uncontrolled hypertension, seizures, uncontrolled diabetes, etc.; Failure to complete a questionnaire and carry out the necessary preliminary examination; The use of steroids and sports supplementation during 3 months ago; Having a regular physical activity program
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Muscle hypertrophy. Timepoint: First and last day of intervention. Method of measurement: Using anthropometry.;Muscle strength. Timepoint: First and last day of intervention. Method of measurement: Using isokinetic.;Range of joint motion. Timepoint: First and last day of intervention. Method of measurement: With a goniometer.;The electrical activity of muscles. Timepoint: First and last day of intervention. Method of measurement: Using EMG. | — |
Secondary
| Measure | Time frame |
|---|---|
| The mean of Quality of life. Timepoint: Baseline, end of 4th week, end of 8th week. Method of measurement: Using WHO quality of life questionnaire.;GH. Timepoint: First and last day of. Method of measurement: Bloodletting.;IGF1. Timepoint: First and last day of. Method of measurement: Bloodletting.;Testosterone. Timepoint: First and last day of. Method of measurement: Bloodletting. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. seyed Kazem Shakouri
Physical Medicine and Rehabilitation group, Tabriz University of Medical Science
Outcome results
None listed