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
  • Other: Kinesiotape
N/A

Detailed Description

30 patients (male and female) suffering from bilateral Halux valgus. Divided randomly into 2 groups

  1. 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.

  2. 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

  1. Hallux valgus angle (HVA ) [8 weeks]

    Hallux valgus angle measured by x ray

  2. 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:

Study Results

No Results Posted as of Dec 21, 2021