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Clinical Trials/NCT06025266
NCT06025266
Completed
Not Applicable

Investigation of the Acute Effect of Foot Extrinsic Muscle Fatigue on Viscoelastic Properties of the Plantar Fascia and Achilles Tendon

Simge Dönmez1 site in 1 country19 target enrollmentOctober 20, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy Participants
Sponsor
Simge Dönmez
Enrollment
19
Locations
1
Primary Endpoint
Biomechanical and viscoelastic properties of tissue
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

In healthy individuals, fatigue in the foot muscles increases the load and stress on the feet. The extrinsic muscles of the foot, which investigators aimed to create fatigue in this study, are closely related anatomically and functionally to the plantar fascia and Achilles tendon. Considering that fatigue or weakness of the foot extrinsic muscles is an important risk factor for foot-ankle pathologies, it is important to reveal the relationship with the plantar fascia and Achilles tendon in healthy sedentary individuals and to determine mechanical properties of the feet of the participants to prevent possible foot injuries. Therefore, the aim of this study is to show the acute effects of fatigue in the extrinsic muscles of the foot on the viscoelastic properties of the plantar fascia and Achilles tendon. The study was completed with 19 people who met the inclusion criteria. Before starting the study, the dominant foot of the participants was determined, physical activity level was determined, foot posture index and foot posture were evaluated, navicular height and fall distance of the foot were measured, m.gastrocnemius shortness was measured with the Silfverskiöld test, flexibility was evaluated with a baseline sitting bench, tendon and fascia measurements were made with the MyotonPRO device. After the measurements, the participant was trained to perform the heel raise exercise. When the exercise was completed, the participant's foot Myoton measurements were repeated. One week later, pre-exercise Myoton measurement was performed, then the participant was trained for the foot adduction exercise. When the exercise was completed, the participant's foot Myotone measurements were repeated. In another week, pre-exercise Myotone measurement was performed, then heel raising and foot adduction exercises were performed sequentially. When the exercise was completed, the participant's foot Myoton measurements were repeated.

Detailed Description

This study was carried out on healthy, sedentary male individuals between the ages of 18-35. In the power analysis to estimate the sample size, Usgu et al. (2020), it was determined that there should be a minimum of 17 observations in each group, with a statistical power level of 82.2% and a significance level of 5%. The study was completed in 3 groups in line with the selected exercises. Firstly, 42 young individuals were included in the study. However, after the preliminary evaluation, 23 individuals who did not meet the inclusion criteria and did not provide continuity to the study were excluded from the study. This study was completed with 19 healthy male individuals with a mean age of 21.37(SD 2.21) years.

Registry
clinicaltrials.gov
Start Date
October 20, 2022
End Date
January 23, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Crossover
Sex
Female

Investigators

Sponsor
Simge Dönmez
Responsible Party
Sponsor Investigator
Principal Investigator

Simge Dönmez

Physiotherapist

Saglik Bilimleri Universitesi

Eligibility Criteria

Inclusion Criteria

  • Agreeing to participate in the study voluntarily
  • Being a healthy, sedentary male individual between the ages of 18 and 35
  • Being in categories 1 and 2 according to the International Physical Activity Survey (UFAA)
  • Having a normal Body Mass Index (BMI) (18.5 kg/m2 ≤ BMI ≤24.9 kg/m2)
  • Having a neutral foot posture (\<6 points in the Foot Posture Index)

Exclusion Criteria

  • Refusing to participate in the study or wanting to leave the study
  • Having a history of previous surgery in the lower extremity
  • Being diagnosed with a musculoskeletal disease
  • Having any chronic disease (hypertension, diabetes, cardiovascular disease, osteoporosis, rheumatism, etc.)
  • Having a skin lesion in the area to be measured
  • Significant weakness in the lower extremity gross muscle test
  • Any limitation in the normal range of motion of the lower extremity
  • Having any deformity in the foot (pes planus, pes cavus, hallux valgus)
  • Navicular drop distance ≥10 mm
  • Limitation in the range of motion of the 1st metatarsophalangeal joint (hallux rigidus-limitus)

Outcomes

Primary Outcomes

Biomechanical and viscoelastic properties of tissue

Time Frame: 3 weeks

Biomechanical and viscoelastic properties of AT and PF were performed using MyotonPro™ (Myoton AS, Tallinn, Estonia) device. Before and immediately after the application of the fatigue protocol, AT and PF measurements were made separately with the MyotonPro™ device. The measurement points determined for AT and PF of individuals during rest were marked with a medical marker pen (16). The measurement points of each person and their distances to the anatomical points were measured with the help of a tape measure and recorded in their files to find the same point again. During the measurement, the probe of the device was adjusted to pulse once into the skin with a force of 0.4 N and for 15 ms. During the test, the tip of the MyotonPro™ device was placed perpendicular to the marked area and gently pressed against the skin at a depth of 3 mm until the green light came on.

Secondary Outcomes

  • Identifying the Dominant Foot(1 day)
  • Sit-Reach Test(1 day)
  • Silfverskiold Test(1 day)
  • Evaluation of Foot Posture(1 day)
  • Navicular Height(1 day)
  • Navicular Drop Distance(1 day)
  • Physical Activity Level(1 day)
  • Evaluation of Fatigue(3 weeks)

Study Sites (1)

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