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The effect of mobilization and soft tissue release of the thoracic on the pain and disability in patients with Total Knee Arthroplasty

The effect of mobilization and soft tissue release of the thoracic on the pain and disability in patients with Total Knee Arthroplasty due to knee Osteoarthritis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230212057390N4
Enrollment
30
Registered
2024-10-02
Start date
2024-10-22
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Damage to the sympathetic nerves. ???? ?? ????? ??????? ???

Interventions

Intervention 1: Intervention group: Performing mobilization and soft tissue release techniques in the thoracic spine region in addition to conventional physiotherapy. Intervention 2: Control group: Co

Sponsors

Mashhad University of Medical Sciences.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients aged between 50 and 80 who have undergone TKA surgery due to severe knee osteoarthritis (1). The TKA surgical method must specifically involve posterior stability. No use of medications affecting the autonomic system, such as psychiatric drugs (21). Pain greater than 3 during functional activities (squatting, stair climbing, and rising from a chair). At least 6 months must have passed since surgery (20). No consumption of alcohol or caffeine for at least 24 hours before the evaluation session (21). Positive result on the Active Standing or Head-Up Tilt test in patients.

Exclusion criteria

Exclusion criteria: Patients with a history of dizziness, mental or cognitive issues, or hearing and speech disorders (20). Patients classified as Red Flag, including those with cancer, infection, or central nervous system disorders (20). History of surgery in the lower limbs, except for TKA surgery (20). Patients with unstable blood pressure (20). History of spinal surgery or fracture. Inability to walk independently. Mechanical and movement issues in the operated knee, such as patellofemoral syndrome or prosthesis dislocation. Smoking or use of any drugs (due to their impact on the autonomic system) (21).

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: First session and tenth session after intervention. Method of measurement: To assess patient pain, the Visual Analogue Scale (VAS) will be used, consisting of a 10-centimeter ruler where individuals rate their pain, with 0 indicating no pain and 10 representing maximum pain (22).;Disability levels. Timepoint: First session and tenth session after intervention. Method of measurement: Disability levels will be evaluated using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), with the validity and reliability of the Persian version confirmed by Eftekharsadat et al. in 2015 (23).

Secondary

MeasureTime frame
Disability levels. Timepoint: First session and tenth session after intervention. Method of measurement: Disability levels will be evaluated using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), with the validity and reliability of the Persian version confirmed by Eftekharsadat et al. in 2015 (23).;Patient satisfaction. Timepoint: First session and tenth session after intervention. Method of measurement: Patient satisfaction post-Total Knee Arthroplasty (TKA) will be assessed using the Oxford Knee Score (OKS), whose Persian version's validity and reliability were established by Ebrahimzadeh et al. in 2014 (24).;Anxiety levels. Timepoint: First session and tenth session after intervention. Method of measurement: Anxiety levels will be evaluated using the Beck Anxiety Inventory (BAI), with the Persian version validated by Kaviani et al. in 2008 (25).;The function of the autonomic system. Timepoint: First session and tenth session after intervention. Method of measurement: The function of the autonomic system will be assessed using the Active Standing test, and if this test is negative, the Head Up Tilt test will be performed (21, 26).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Shahbazi.

Mashhad University of Medical Sciences

shahbazim2@mums.ac.ir+98 915 522 8949

Outcome results

None listed

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