People with upper cross syndrome. Personal history of other specified conditions
Conditions
Interventions
Intervention 1: Intervention group: The moderate porticul intervention group performs 3 sessions per week for 6 weeks. Intervention 2: Control group: There is no intervention.
Sponsors
Rasht University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 25 Years
Inclusion criteria
Inclusion criteria: Round shoulder > 52 degree, Forward head > 46 degree , Kyphosis > 42 degree Not having surgery history in the past year The absence of anomalies affecting the research process
Exclusion criteria
Exclusion criteria: use of drugs that affect the balance
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Balance. Timepoint: Measurement of balance tests before and after 6 weeks of intervention. Method of measurement: Functional test of balance.;Postural status. Timepoint: Measure postural status before and after 6 weeks of intervention. Method of measurement: Check for shoulder belt postural. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life. Timepoint: Assessing the quality of life before and after 6 weeks of intervention. Method of measurement: Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFariba Javazi
Rasht University of Medical Sciences
Outcome results
None listed