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NCT02772042 Clinical Trial

Traction Manipulation of Upper Cervical Spine on Cervicogenic Dizziness

Neck Pain Clinical Trial

Official title:
Effectiveness of Traction Manipulation of Upper Cervical Spine on Cervicogenic Dizziness

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02772042
Other study ID # PI15/0230
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2015
Est. completion date May 2017

Study information
Verified date May 2018
Source Universidad de Zaragoza
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Manual therapy reduces symptoms in patients with cervicogenic dizziness. The mobilization and manipulation of upper cervical spine are the most popular treatment in this patients. The International Federation of Orthopaedic Manipulative Physical Therapists suggest different recommendations for the safety application of manual therapy techniques in the upper cervical spine, traction manipulation techniques complies with this conditions. However, there isn´t investigation about the effect of traction manipulation in patients with cervicogenic dizziness. The aim of this study is to investigate the effects of traction manipulation in dizziness intensity, range of motion of cervical spine and quality of life on patients with cervicogenic dizziness.

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date May 2017
Est. primary completion date November 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Dizziness associated with neck stiffness and/or neck pain.

- Hypomobility of upper cervical spine.

- Sing the informed consent form.

Exclusion Criteria:

- Contraindications for Traction manipulation.

- Pending litigation or legal claim.

- Poor language and communication skills making difficult to understand the informed consent.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Intervention Group

• Control Group

Locations
Country Name City State
Spain Unidad de Investgación en Fisioterapia. Universidad de Zaragoza Zaragoza

Sponsors (1)
Lead Sponsor Collaborator
Andoni Carrasco

Country where clinical trial is conducted

Spain, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change of baseline in Dizziness Intensity (100mm VAS) at 1 week and 1 month Baseline- 1 week- 1 month
Secondary Change of baseline in range of motion of cervical spine change (Tool: Cervical range of motion) Baseline- 1 week- 1 month
Secondary Change of baseline in upper cervical spine range of motion (Tool: Cervical range of motion) Baseline- 1 week- 1 month
Secondary Change of baseline in dizziness Handicap Inventory (questionnaire) Baseline- 1 week- 1 month
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