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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03154853
Other study ID # 201607074RINB
Secondary ID
Status Recruiting
Phase N/A
First received May 8, 2017
Last updated May 21, 2017
Start date November 4, 2016
Est. completion date December 30, 2017

Study information

Verified date May 2017
Source National Taiwan University Hospital
Contact Jen Yu Chen, Ph.D.
Phone +886-2-33668138
Email yujensch@ntu.edu.tw
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purposes of these studies are to investigate:

Differences in abductor hallucis muscles'EMG activities during different postural tasks between individuals with normal foot alignment and functional flat foot. Differences in abductor hallucis muscles'H-reflex amplitudes between individuals with normal foot alignment and functional flat foot. Changes in abductor hallucis muscles'EMG activities during different postural tasks after a 3-week short foot exercises training regimen in individuals with functional flat foot. Changes in abductor hallucis muscles'H-reflex amplitudes after a 3-week short foot exercises training regimen in individuals with functional flat foot. hypotheses: Peak-to-peak amplitudes and ratios of abductor hallucis muscles and tibialis anterior muscles during different postural tasks were significantly lower in individual with functional flat foot when compared to those with normal foot alignments. H-reflex amplitudes of abductor hallucis muscles were significantly lower in individual with functional flat foot when compared to those with normal foot alignments. Changes of peak-to-peak amplitudes and ratios of abductor hallucis muscles and tibialis anterior muscles during different postural tasks were significantly different in individuals with functional flat foot after a 3-week short foot exercise training regimen. Changes of H-reflex amplitudes of abductor hallucis muscles were significantly different in individuals with functional flat foot after a 3-week short foot exercise training regimen


Recruitment information / eligibility

Status Recruiting
Enrollment 45
Est. completion date December 30, 2017
Est. primary completion date September 30, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 45 Years
Eligibility : Inclusion Criteria:

- Age between 20 and 45 years

- No ankle injury within the previous 6 months

- No diagnosed lower extremity injuries

- No ankle pain at the time of the study

- Foot posture index score: 0 to +5 for the normal foot (NF) group; +6 to +12 for the functional flat foot (FFF) group

- Navicular drop: 5-9 mm for the NF group; > 10 mm for the FFF group

Exclusion Criteria:

- Foot posture index score: <0

- Navicular drop< 5 mm

- Leg length discrepancy > 1.5 cm

- Diagnosed severe scoliosis

- Neurological injuries over lower extremities

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Behavioral: short foot exercise
Behavioral: short foot exercise 30 repetitions per section (10 seconds for each contraction, 1 minute between sections), 3 times/ week, 3 weeks

Locations

Country Name City State
Taiwan National Taiwan University Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle activities: EMGs (mV) EMGs (mV) in each posture Baseline
Primary Muscle activities: H-reflexes (mV) H-reflexes (mV) in each posture Baseline
Primary Muscle activities change will being assessed: EMGs (mV) EMGs (mV) in each posture Baseline. week 3
Primary Muscle activities change will being assessed: H-reflexes (mV) H-reflexes (mV) in each posture Baseline. week 3
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