RCT: Hallux Valgus Conservative Treatment
Sponsor
University of Jazan (Other)
Overall Status
Completed
CT.gov ID
NCT05165134
Collaborator
(none)
30
1
2
14.7
2
Study Details
Study Description
Brief Summary
Studying the effect of kinesiotape on hallux valgus angle and pain in hallux valgus patients.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
N/A |
Detailed Description
30 patients (male and female) suffering from bilateral Halux valgus. Divided randomly into 2 groups
-
st group receive kinesiotape bilaterally for correction : Hallux valgus angle (HVA) was measured using Xray and pain was measured using VAS before applying tape and after 8 weeks of tape application.
-
nd group receive placebo tape bilaterally and had the same measurements.
2 groups were on a group of exercises
Study Design
Study Type:
Interventional
Actual Enrollment
:
30 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Pretest and posttest Control group randomized control trialPretest and posttest Control group randomized control trial
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Influence of Short-Term Conservative Treatment Using Kinesiotape on Hallux Valgus Angle
Actual Study Start Date
:
Aug 24, 2020
Actual Primary Completion Date
:
Jan 29, 2021
Actual Study Completion Date
:
Nov 15, 2021
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Experimental: Experimental kinesiotape group A Kinesiotape group |
Other: Kinesiotape
Elastic tape used for mechanical correction of the deformity in study group and placebo in control group
|
Placebo Comparator: Placebo kinesiotape group B Control group |
Other: Kinesiotape
Elastic tape used for mechanical correction of the deformity in study group and placebo in control group
|
Outcome Measures
Primary Outcome Measures
- Hallux valgus angle (HVA ) [8 weeks]
Hallux valgus angle measured by x ray
- Pain on metatarsophalangeal joint measured by visual analogue scale (VAS) [8 weeks]
Eligibility Criteria
Criteria
Ages Eligible for Study:
20 Years
to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
- mobile hallux valgus
Exclusion Criteria:
-
using orthotics
-
knee malalignment
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Jazan University | Gizan | Jazan | Saudi Arabia | 45142 |
Sponsors and Collaborators
- University of Jazan
Investigators
- Principal Investigator: Mohamed M Ahmed, Assistant Professor of physical therapy
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Mohammed Moustafa,
assistant Professor of physical therapy,
University of Jazan
ClinicalTrials.gov Identifier:
NCT05165134
Other Study ID Numbers:
- JU
First Posted:
Dec 21, 2021
Last Update Posted:
Dec 21, 2021
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: