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Investigating the effects of exercise and self-management education on pain and function in patients with avascular necrosis of the femoral head

Investigating the effect of mixed therapeutic exercises and self-management education with and without functional strength exercises on pain and function factors in patients with avascular necrosis of the femoral head

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220510054814N2
Enrollment
53
Registered
2023-05-30
Start date
2023-06-22
Completion date
Unknown
Last updated
2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Avascular necrosis of the femoral head. Osteonecrosis

Interventions

Intervention 1: Control group: Mixed therapeutic exercises: Both groups present in this research will receive the Mixed therapeutic exercises protocol. In this way, after registering the demographic i

Sponsors

Kharazmi University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Diagnosis of osteonecrosis of the femoral head according to the diagnostic criteria of AVN from grade I to IV (based on ARCO classification criteria) Hip pain/ decreased mobility Ability to read and write and access to a smartphone or tablet Age over 18 years

Exclusion criteria

Exclusion criteria: Participation in a physical therapy program, and regular exercise therapy during the last 6 months Being on the waiting list for joint replacement surgery (in the next 3 months) Hip/ knee replacement surgery Patients who cannot complete therapeutic exercises for a period of three months Severe osteoporosis Severe medical, neurological, or psychiatric conditions Failure to fill out the consent form Severe osteonecrosis of the knee/ severe knee osteoarthritis

Design outcomes

Primary

MeasureTime frame
Pain and pain in functional activities. Timepoint: Will be measured at the baseline, after the end of 3 months intervention, and after the end of 4 months follow up. Method of measurement: Using a 10 cm numeric pain rating scale during walking and sitting to stand, also pain for the last two weeks.

Secondary

MeasureTime frame
Measure of dysfunction. Timepoint: Will be measured at the baseline, after the end of 3 months intervention, and after the end of 4 months follow up. Method of measurement: Harris Hip Score.;Pain, stiffness and physical function. Timepoint: Will be measured at the baseline, after the end of 3 months intervention, and after the end of 4 months follow up. Method of measurement: Western Ontario and McMaster Universities Osteoarthritis index in hip osteoarthritis.;Physical function. Timepoint: Will be measured at the baseline, after the end of 3 months intervention, and after the end of 4 months follow up. Method of measurement: Timed up and go (TUG); 30-s chair-stand test.;Joints range of motion. Timepoint: Will be measured at the baseline, after the end of 3 months intervention, and after the end of 4 months follow up. Method of measurement: Goniometer.;Muscles strength. Timepoint: Will be measured at the baseline, after the end of 3 months intervention, and after the end of 4 months follow up. Method of measurement: Hand-held dynamometer.;Walking speed. Timepoint: Will be measured at the baseline, after the end of 3 months intervention, and after the end of 4 months follow up. Method of measurement: 10-meter walk test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohre Gholami

Kharazmi University

Zzohreh.Ggholami@gmail.com+98 21 2222 8001

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026