Manual Therapy to Treat Acute Whiplash Injury
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|ClinicalTrials.gov Identifier: NCT01825460|
Recruitment Status : Completed
First Posted : April 5, 2013
Last Update Posted : September 24, 2013
|Condition or disease||Intervention/treatment|
|Whiplash Injuries||Other: Manual Therapy Protocol Other: Two manual techniques|
Design: Randomized clinical trial. Objectives: to determine the short-term effects of a a manual therapy protocol on pain, disability and cervical range of motion in individuals with acute whiplash injury.
Methods and measures: sixty patients will be randomly assigned to 1 of 2 groups: the experimental group received a manual therapy protocol and the placebo group received two manual therapy techniques. Neck pain, disability and cervical range of motion data will be collected at baseline and 24-hr after the last manual therapy application. Mixed-model analyses of variance will be used to examine the effects of the treatment on each outcome variable.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||60 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||Double (Participant, Outcomes Assessor)|
|Official Title:||Short-Term Effects of a Manual Therapy Protocol|
|Study Start Date :||April 2013|
|Primary Completion Date :||September 2013|
|Study Completion Date :||September 2013|
Experimental: Manual Therapy Protocol
A protocol with five techniques on thoracic area applied twice a week.
Other: Manual Therapy Protocol
The manual therapy protocol consists in the application of the following techniques: stretching diaphragm, Inhibition for phrenic center, Neuromuscular technique, technique jones and balance technique functional.
Active Comparator: Two manual techniques
Two manual therapies on thoracic area applied twice a week.
Other: Two manual techniques
The two manual techniques applied to control group are: inhibition for phrenic center and neuromuscular technique.
- Change on Numerical Pain Rating Scale [ Time Frame: At baseline and 2 weeks ]The numerical pain rating scale is used to record the patient´s current level of neck pain.
- Neck disability index [ Time Frame: At baseline and 2 weeks ]The neck disability index consists of 10 questions addressing functional activities such as personal care, lifting, reading, work, driving, sleeping, recreational, pain intensity, concentration and headache.
- Cervical Range of Motion [ Time Frame: At baseline and 2 weeks ]Cervical range of motion is assessed with the patient sitting comfortably on a chair, with both feet flat on the floor, hips and knees at 90º of flexion, and buttocks positioned against the back of the chair.
- Tampa scale for kinesiophobia [ Time Frame: At baseline and 2 weeks ]The 17-item Tampa scale for kinesiophobia assesses fear of movement or of injury or reinjury.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01825460
|Adelaida María Castro-Sánchez|
|Almeria, Spain, 04120|
|Study Director:||Adelaida M Castro-Sánchez, PhD||Universidad de Almeria|