Rheumatoid arthritis. Rheumatoid arthritis with rheumatoid factor, unspecified
Conditions
Interventions
Intervention 1: Intervention group: In group 1 (intervention), the walking protocol will be conducted for 30 sessions within 8 consecutive weeks (First and second week five days a week, third and four
Behavior
Intervention group: In group 1 (intervention), the walking protocol will be conducted for 30 sessions within 8 consecutive weeks (First and second week five days a week, third and fourth week four day
Control group: In group 2 (control), people will not receive any interventions.
Sponsors
Yasouj University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: Patient with Rheumatoid arthritis and diagnosis by rheumatologist. The patient will be treated and have a medical record. Age of Pre-menopause (20-50 years) There is no underlying disease; infectious diseases and and diseases of the genital apparatus No participation in sports activities in the last three years A score of less than 26/5 in the Rosen Gender Indicator Questionnaire Absence in the acute phase of the disease Not giving birth in the last six months and not getting pregnant Confirmation of the patient by the physician to participate in the walking exercise Passed at least one year from the diagnosis of joint rheumatoid arthritis by a doctor No use of sex hormones supplements affecting sexual desire
Exclusion criteria
Exclusion criteria: The patient's unwillingness to continue attending this research Lack of attendance for more than two sessions Disturbance in cognitive status and patient's alertness and balance during intervention Separating from his wife Getting pregnant Immigration or death Patient's menopausal during the intervention Other illness Transfer to another Medical center Re-enter the acute phase of the disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual function. Timepoint: Before the intervention, the end of the eighth week and performing two or three intercourse after the end of the intervention. Method of measurement: Women's Sexual Function Inventory. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSima Mohammad Hosseini
Yasouj University of Medical Sciences
Outcome results
None listed