Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
60 participants
INTERVENTIONAL
2019-09-01
2020-03-25
Brief Summary
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Detailed Description
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Initially, the base measurements were as follows: paint intensity, pressure pain threshold at the gluteus medius trigger point, ankle range of motion and balance of the lower limb.
Once baseline measurements will be taken, the same evaluations will be performed at 4 weeks from the start.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Intervention group
Individuals for this group will be treat with a dry needling intervention at the gluteus medius trigger point.
Dry needling
For this intervention, the physiotherapist will be placed a needle in the gluteus medius trigger point from 8 to 15 times.
Control group
Individuals for this group will be treat with a dry needling technique at 1,5 cm from the trigger point (not in the trigger point).
Dry needling
For this intervention, the physiotherapist will be placed a needle in the gluteus medius trigger point from 8 to 15 times.
Interventions
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Dry needling
For this intervention, the physiotherapist will be placed a needle in the gluteus medius trigger point from 8 to 15 times.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
50 Years
ALL
No
Sponsors
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Universidad Europea de Madrid
OTHER
Responsible Party
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Carlos Romero Morales
Principal Investigator
Locations
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Fiom clinic
Madrid, , Spain
Countries
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Other Identifiers
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CIPI/19/012
Identifier Type: -
Identifier Source: org_study_id
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