Fear of COVID-19, kinesiophobia, number of step, pain, dyspnea and quality of life in individuals with idiopathic scoliosis
- Conditions
- Fear of contracting COVID-19KinesiophobiaLow step countPain perceptionDyspnea perceptionPoor quality of lifeidiopathic scoliosisMusculoskeletal - Other muscular and skeletal disorders
- Registration Number
- ACTRN12622000178741
- Lead Sponsor
- GÜLSAH BARGI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 58
• Adult individuals aged 18 and over
• Individuals who volunteered to participate in the study
• Individuals diagnosed with idiopathic scoliosis
• Individuals who can walk independently
• Individuals who have undergone scoliosis surgery
• Individuals with mental problems that may affect cooperation
• Individuals with acute or chronic infections that may affect the evaluations to be made within the scope of the study.
• Individuals participating in any professional sporting activity
• Individuals who have undergone any surgery to prevent walking, have chronic illness, physical or mental disability and/or cognitive impairment, orthopedic/neurological/cardiopulmonary disorders
• Individuals who have had COVID-19
• Individuals diagnosed with COVID-19 (Positive Polymerase Chain Reaction (PCR) test results, those with negative PCR test results but compatible with COVID-19 infection with chest X-ray or lung tomography results)
• Individuals with suspected COVID-19
• Pregnant women
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The status of quality of life which will be evaluated using Scoliosis Research Society-22 (SRS-22) questionnaire.[at survey time]
- Secondary Outcome Measures
Name Time Method Fear of contracting COVID-19 which will be evaluated using the Fear of COVID-19 Scale.[at survey time];Presence of kinesiophobia which will be evaluated using Tampa Kinesiophobia Scale.[at survey time];Daily step counts: Daily average step counts during 3 days will be recorded via pedometer applications installed on smartphones. All patients will be asked to carry their smartphones with them during the day and record to their diaries.[at survey time, within 3 days after confirming enrolment];Pain perception which will be evaluated using Numerical Rating Scale[At survey time];Dyspnea perception which will be evaluated using Numerical Rating Scale[At survey time]