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Manual Therapy to Treat Acute Whiplash Injury

Not Applicable
Completed
Conditions
Whiplash Injuries
Interventions
Other: Two manual techniques
Other: Manual Therapy Protocol
Registration Number
NCT01825460
Lead Sponsor
Universidad de Almeria
Brief Summary

The purpose of this study is to determine the short-term effects of a manual therapy protocol on pain, disability and cervical range of motion in individuals with acute whiplash injury.

Detailed Description

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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • To met Quebec Task Force Classification of WAD II- neck pain symptoms and musculoskeletal signs.
  • No evidence of conduction loss on clinical neurological examination.
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Exclusion Criteria
  • Concussion during the motor vehicle accident.
  • Loss of consciousness.
  • Head or upper quadrant injury during the accident.
  • Sought treatment prior to their accident for neck pain.
  • A previous history of whiplash
  • Neck pain
  • Headaches
  • Psychiatric or psychologic condition
  • Neurologic or circulatory disorders
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Two manual techniquesTwo manual techniquesTwo manual therapies on thoracic area applied twice a week.
Manual Therapy ProtocolManual Therapy ProtocolA protocol with five techniques on thoracic area applied twice a week.
Primary Outcome Measures
NameTimeMethod
Change on Numerical Pain Rating ScaleAt baseline and 2 weeks

The numerical pain rating scale is used to record the patient´s current level of neck pain.

Secondary Outcome Measures
NameTimeMethod
Neck disability indexAt 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 MotionAt 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 kinesiophobiaAt baseline and 2 weeks

The 17-item Tampa scale for kinesiophobia assesses fear of movement or of injury or reinjury.

Trial Locations

Locations (1)

Adelaida María Castro-Sánchez

🇪🇸

Almeria, Spain

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