N/A
N=22
Initial Effects of Kinesiotaping in Non Surgical Treatment of Hallux Valgus
Hallux Valgus · Pain
Bottom Line
View on ClinicalTrials.gov: NCT01952691 ↗Enrolled (actual)
22
Serious AEs
0.0%
Results posted
Apr 2015
Primary outcome: Primary: Adduction Angle of Hallux With X RAY — 22.6; 19.3 degrees
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- kinesiotaping (Device)
- Age
- Adult · 18+ yrs
- Sex
- Female
- Sponsor
- Hacettepe University
- Primary completion
- Oct 2011
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Adduction Angle of Hallux With X RAY |
22.6; 19.3 | — |
| SECONDARY FFI |
3.2; 0.84 | — |
| SECONDARY Adduction Angle |
20.2; 14.3 | — |
Summary
The main aim of this study was to find the initial effects of kinesiotaping on pain and joint alignment used in the conservative treatment of hallux valgus.
22 female patients diagnosed with hallux valgus participated in this study. Kinesiotaping was implemented after the first assessment and renewed in the 3rd, 7th and 10th days. The main outcome measures were the pain hallux adduction angle. Kinesiotaping may be an effective treatment option in decreasing pain and deformity in hallux valgus deformity who are conservatively treated. In future studies this method might be shown in larger sample groups at longer periods of treatment comparing with alternative treatment approaches like exercise or orthotics.
Eligibility Criteria
Inclusion Criteria
- Hallux adduction angle between 15-40º
- Pain intensity higher than 5 according to VAS
- 20- 45 years age female
- No trauma, surgery history
- Surgery is indicated but the patient is willing to try conservative treatment options
Exclusion Criteria
- Fracture, surgery history on the great toe
- Systematic disease (Rheumatoid Arthritis, Systematic Lupus Erythematosus Diabetes)
- Using NSAID, analgesic drug
- Hallux rigidus diagnosis
Data sourced from ClinicalTrials.gov (NCT01952691). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.