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Mold Making Silicone Toe Separator on Hallux Valgus

Not Applicable
Conditions
Hallux Valgus
Interventions
Device: Mold making silicone toe separator
Other: Observation
Registration Number
NCT02220881
Lead Sponsor
Mahidol University
Brief Summary

The primary objective of this study is to investigate the effectiveness of mold making silicone toe separator on reducing the hallux valgus angle. In addition, this study aims to determine the compliance of mold making silicone toe separator, the change in pain level and, including, the satisfaction of the participants after using mold making silicone toe separator.

Detailed Description

Study Protocol, Data collection

Ninety recruited sample is the patient come to the foot clinic, Siriraj Hospital with the age over eighteen years old, presence of hallux valgus deformity in moderate level (without the condition of hallux rigidus), and never use hallux valgus strap or toes separator before.

The sample is given a physical assessment by physician and is asked to fill in a self-administered questionnaire which composes of general information, the foot problem information and the impact of deformity to patients function information. General information section requires the detail regarding age, genders, and the average walking hours. Foot problem information section composes of side, duration of hallux valgus and family history. Impacts of the hallux valgus deformity section includes walking problem, shoes-fitting problem, working problem, and daily activities problem, were recorded by using a numeric rating scale from 0 to 10; 0 refers as no problem and 10 refers as the worst problem. The sample then will be taken the radiograph of the feet in order to evaluate the degree of hallux valgus angle and intermetatarsal angle.

After the completion of assessment, the sample is randomly divided into 2 groups; control and experimental group by using computer program.

* Control group receives the recommendation of use the proper shoes without determination of current drug use

* Experimental group receives the custom-made mold making silicone toe separator made by certified orthotist and the recommendation of use the proper shoes without determination of current drug use

The follow up activity is on every 3rd, 6th, 9th and 12th of the study period in both groups by using questionnaire; pain score (NRS), satisfaction of using the custom-made mold making silicone toe separator (NRS) and report of complication. In the 6th and 12th month, the progress evaluation on hallux valgus and intermetatarsal angle is done by radiograph. The angle then is recorded by mean of the three values.

Descriptive statistics; mean, standard deviation or interquartile range, will be used to identify the demographic data of the participant and compliance of device usage. Analytical statistics; Unpaired t-test or Mann Whitney U test will be used for determining the average device usage time, pain score, and satisfaction of the participants after using mold making silicone toe separator.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
90
Inclusion Criteria
  • More than 18 years of age
  • Presence of hallux valgus deformity in moderate level, if the condition presents in both side, the one with greater angle will be selected
  • Never use hallux valgus strap or toes separator before
Exclusion Criteria
  • Presence of hallux rigidus and hallux limitus
  • Presence of acute hallux inflammation
  • Experience the use hallux valgus strap or toes separator in a past year
  • Experience the allergy to silicone

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Mold making silicone toe separatorMold making silicone toe separatorThe subject in experimental group will use mold making silicone toe separator everyday
ObservationObservationThis group will follow the physician instruction of care for the hallux valgus
Primary Outcome Measures
NameTimeMethod
Change from baseline of degree of intermetatarsal angle at month 6 ans month 12Baseline, month 6, month 12

Intermetatarsal angle will be measured from the x-ray film taken in standing position with full weight bearing

Change from baseline of degree of Hallux valgus angle at month 6 ans month 12Baseline, month 6, month 12

Hallux valgus angle will be measured from the x-ray film taken in standing position with full weight bearing

Secondary Outcome Measures
NameTimeMethod
Change from baseline in pain score on 11-point Visual Analog Scale at month 3, month 6, month 9 and month 12Baseline, month 3, month 6, month 9 and month 12

To measure the pain score of the hallux by using the numeric rating scale in the 3rd, 6th, 9th and 12th month

Trial Locations

Locations (1)

Faculty of Medicine Siriraj Hospital

🇹🇭

Bangkok-noi, Bangkok, Thailand

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