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Clinical Trials/NCT01825460
NCT01825460CompletedNot Applicable

Short-Term Effects of a Manual Therapy Protocol

Universidad de Almeria2 sites in 1 country60 target enrollmentStarted: April 2013Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
60
Locations
2
Primary Endpoint
Change on Numerical Pain Rating Scale

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
25 Years to 50 Years (Adult)
Sex
All
Accepts 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

Outcomes

Primary Outcomes

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.

Secondary Outcomes

  • Neck disability index(At baseline and 2 weeks)
  • Cervical Range of Motion(At baseline and 2 weeks)
  • Tampa scale for kinesiophobia(At baseline and 2 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Adelaida María Castro-Sánchez

PhD (Lecturer)

Universidad de Almeria

Study Sites (2)

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