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Manual Therapy to Treat Acute Whiplash Injury

Short-Term Effects of a Manual Therapy Protocol

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01825460
Enrollment
60
Registered
2013-04-05
Start date
2013-04-30
Completion date
2013-09-30
Last updated
2013-09-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Whiplash Injuries

Keywords

Cervical spine, Neck pain, Manual therapy, Controlled clinical trial

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.

Interventions

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.

OTHERTwo manual techniques

The two manual techniques applied to control group are: inhibition for phrenic center and neuromuscular technique.

Sponsors

Universidad de Granada
CollaboratorOTHER
Universidad Rey Juan Carlos
CollaboratorOTHER
Universidad de Almeria
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
25 Years to 50 Years
Healthy volunteers
No

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.

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

Design outcomes

Primary

MeasureTime frameDescription
Change on Numerical Pain Rating ScaleAt baseline and 2 weeksThe numerical pain rating scale is used to record the patient´s current level of neck pain.

Secondary

MeasureTime frameDescription
Neck disability indexAt baseline and 2 weeksThe 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 weeksCervical 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 weeksThe 17-item Tampa scale for kinesiophobia assesses fear of movement or of injury or reinjury.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026