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Kineesiotaping for Patients With LCPD

Effects of Kinesiotaping in Patients With Legg-Calvé-Perthes Disease: A Randomized, Double-blind, Placebo-controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05840146
Enrollment
30
Registered
2023-05-03
Start date
2017-09-25
Completion date
2021-01-11
Last updated
2023-05-03

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

Conditions

Legg-Calve-Perthes Disease

Keywords

Kinesiotape, Taping, Pediatric pain, Hip joint, Physiotherapy

Brief summary

Kinesiotaping is increasingly being used as a complement to musculoskeletal pain management. This study aimed to evaluate the immediate clinical efficacy of kinesiotaping on pain and pain-related symptoms of Legg-Calvé-Perthes Disease (LCPD).

Detailed description

Kinesio taping is increasingly being used as a complement to musculoskeletal pain management. A randomized, double-blind, placebo-controlled clinical trial was conducted. Activity-related hip pain, passive and pain limited hip range of motion, gluteus medius muscle strength, function and balance were assessed.

Interventions

OTHERKinesiotaping

Two I-strips were used: 1. The first-third of one I-strip began at the posterior iliac crest, without tension as an anchor. Then the patient actively flexed and adducted the affected hip, thus, the middle-third of the tape was applied with approximately 50% tension. Then the hip was set in its original position and the last-third of the tape ended approximately greater trochanter without tension. 2. The first-third of the second I-strip was applied starting at the anterior iliac crest, without tension as an anchor. The patient actively extended and adducted the affected hip, thus, the middle-third of the tape was applied with approximately 50% tension. Then the hip was set in its original position and the last-third of the tape ended approximately greater trochanter without tension.

OTHERSham taping

A single I-strip without tension in tape or muscle stretch. After paper backing was completely removed, tape was essentially placed on the skin across the lateral side of the hip.

Sponsors

Istanbul University - Cerrahpasa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
5 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Having received unilateral LCPD diagnosis, * Anterior hip pain minimum three points on 10-cm Visual Analog Scale (VAS) over the previous week, * Having the following symptoms; weakness of gluteus medius muscle and patient-reported complaints on function or balance

Exclusion criteria

* Having a history of any other hip pathologies, * Having allergy to polyacrylate adhesive, * Having used analgesic medication within the previous three days.

Design outcomes

Primary

MeasureTime frameDescription
Immediate Clinical Efficacy on Activity Related HipThe change between T1 (baseline) to T2 (thirty minutes later from the application)Horizontal 10 cm VAS (0, no pain; 10, the worst pain ever possible)

Secondary

MeasureTime frameDescription
Immediate Clinical Efficacy on Hip Abduction ROMThe change between T1 (baseline) to T2 (thirty minutes later from the application)goniometric range of motion (ROM)
Immediate Clinical Efficacy on Functional Task DurationsThe change between T1 (baseline) to T2 (thirty minutes later from the application)10-meters walk task duration (sec) and 10-step climbing task duration (sec)
Immediate Clinical Efficacy on Balance test durationsThe change between T1 (baseline) to T2 (thirty minutes later from the application)One leg stance test duration (sec) and Tandem walk test duration (sec)
Immediate Clinical Efficacy on Gluteus medius muscle strengthThe change between T1 (baseline) to T2 (thirty minutes later from the application)muscle strength by handheld dynamometer (Ibs)

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026