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OpenTrials
Completed

NCT Number: NCT01989338

Effects of Hallux Valgus Deformity on Rear Foot Position, Pain, Function, and Quality of Life in Women

To investigate relationship between HV deformity and position of rearfoot joints, and its effects on the quality of life, pain, and related functional status in women with bilateral hallux valgus (HV).

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Key information

About this study

To investigate relationship between HV deformity and position of rearfoot joints, and its effects on the quality of life, pain, and related functional status in women with bilateral hallux valgus (HV). Study included 27 right-dominant women. Demographic data, HV angle, weight-bearing and non-weight-bearing subtalar pronation (SP), and navicular height were recorded. Visual Analog Scale, Foot Function Index (FFI), and the American Orthopaedic Foot and Ankle Society (AOFAS) MTP-IP along with AOFAS Mid foot (MF) Scales, and SF-36 were used. HV angle, weight-bearing SP, and pain intensity of the left foot were higher. HV angle of left foot was correlated with all sub-sections of FFI, pain parameter of AOFAS MTP-IP, and pain and total score of AOFAS-MF Scale ). HV angle of left foot was correlated with physical role, pain, and social function sub-domains of SF-36. Right HV angles were correlated with right foot pain and non-weight-bearing SP.Increasing HV angle and pathomechanical changes in rear foot were correlated. Besides, although all participants were right-dominant, their left foot problems were more highlighted.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Inclusion criteria were as follows:

  • Women in an age range of 18-55 years,
  • Having bilateral deformity with right-dominance,
  • First MTP angle of > 15° as radiologically determined by the referring physician,
  • Deformity intensity > 2 based on the Manchester scale,
  • Muscle forces on ankle and foot > 4
  • Having no systemic disease that affects foot biomechanics with no history of surgery,
  • Having no neurological problems,
  • Having no cognitive, mental, or psychological problems.

Exclusion criteria

-

Treatment and study plan

Primary outcomes

  1. Pain

    Time frame: baseline

    Pain was measured using by Visual Analog Scale

  2. AOFAS Mid foot (MF) Scales

    Time frame: baseline

Secondary outcomes

  1. HV angle and navicular height

    Time frame: baseline

    HV angle was measured by using Universal Goniometers

Other outcomes

  1. Foot Function Index

    Time frame: baseline

    Using the Foot Function Index

  2. American Orthopaedic Foot and Ankle Society (AOFAS)MTP-IP

    Time frame: baseline

  3. weight-bearing and non-weight-bearing subtalar pronation (SP)

    Time frame: baseline

  4. SF-36

    Time frame: baseline

Sponsors and collaborators

Lead sponsor

Hacettepe University

Other

Registry information

Important dates

Study start
2012
Primary completion
2012
Study completion
2013
First posted
Nov 21, 2013
Registry last updated
Nov 21, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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