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
50 participants
INTERVENTIONAL
2019-06-11
2019-09-11
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Active intervention
Patients will be included in an active intervention.
Active exercising
Patients allocated to the experimental group were included in an active exercising program adapted to each patient
Control group
Patients in the control group will not receive any intervention
No interventions assigned to this group
Interventions
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Active exercising
Patients allocated to the experimental group were included in an active exercising program adapted to each patient
Eligibility Criteria
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Inclusion Criteria
* Neck pain of at least 3 on a visual analogue scale.
* Participants' symptoms should be at least partly related to increased nerve mechanosensitivity in the neck and upper limb confirmed by the reproduction of participants' symptoms by median nerve upper-limb neurodynamic test.
Exclusion Criteria
* Previous cervical surgical intervention.
* Cognitive impairments which prevent them to follow instructions.
* Visual or acoustic limitations.
18 Years
65 Years
ALL
No
Sponsors
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Universidad de Granada
OTHER
Responsible Party
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Marie Carmen Valenza
Principal Investigator
Locations
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Department of Physical Therapy
Granada, , Spain
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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DF0081UG
Identifier Type: -
Identifier Source: org_study_id
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