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Clinical Trials/NCT03502928
NCT03502928CompletedNot Applicable

Efficacy of the Use of Dry Needling in Conventional Non-invasive Treatment of Acute and Subacute Whiplash

University of Alcala1 site in 1 country30 target enrollmentStarted: November 4, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
Neck Disability Index. Changes from Baseline

Study Overview

Brief Summary

INTRODUCTION: Whiplash is an injury produced by an acceleration-deceleration mechanism that transmits energy to the cervical spine. According to the bibliography, the conservative treatment (motor control exercises and manual therapy) has shown benefits in approaching this lesion, but its efficacy is limited. Dry needling has already shown its usefulness in different musculoskeletal pathologies, however, its efficacy is unknown when it is included in conservative treatment.

OBJECTIVES: The objective of this study is to assess the effects of the incorporation of dry needling in the conventional treatment with manual therapy and motor control exercises, compared to the conventional non-invasive treatment in patients with acute or subacute whiplash.

HYPOTHESIS: The inclusion of dry needling in conventional non-invasive treatment is more effective than conventional non-invasive treatment in patients with acute or subacute whiplash.

METHODS: A randomized clinical trial will be conducted in which the subjects of study will be assigned to two groups, a control group (conventional treatment) and an experimental group (conventional treatment and dry needling).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Medical Diagnosis of Whiplash Grade I-II in the QTF
  • •Neck Pain
  • •Whiplash in Acute or Subacute Phase

Exclusion Criteria

  • •Pregnancy
  • •Belonephobia
  • •Cervical Fractures-Dislocations or Neurological Deficit Secondaries to Accident
  • •Previous Surgery of the Cervical Spine
  • •Circulatory Disease, Respiratory Disease, Neurological Disease, Rheumatologic Disease and Mental Illness

Arms & Interventions

Experimental Treatment

Experimental

Motor Control + Manual Therapy + Dry Needling

Intervention: Dry Needling (Other)

Experimental Treatment

Experimental

Motor Control + Manual Therapy + Dry Needling

Intervention: Manual Therapy (Other)

Conventional Treatment

Active Comparator

Motor Control + Manual Therapy

Intervention: Motor Control (Other)

Conventional Treatment

Active Comparator

Motor Control + Manual Therapy

Intervention: Manual Therapy (Other)

Experimental Treatment

Experimental

Motor Control + Manual Therapy + Dry Needling

Intervention: Motor Control (Other)

Outcomes

Primary Outcomes

Neck Disability Index. Changes from Baseline

Time Frame: 3 weeks, 6 weeks, 3 months

0-100% (0% = No Disability; 100% = Disability (highest level of disability)

Secondary Outcomes

  • Pressure pain thresholds. Changes from Baseline(3 weeks, 6 weeks, 3 months)
  • Cervical Range of Movement. Changes from Baseline(3 weeks, 6 weeks, 3 months)
  • Kinesophobia. Changes from Baseline(3 weeks, 6 weeks, 3 months)
  • Cervical Motor Control. Changes from Baseline(3 weeks, 6 weeks, 3 months)

Investigators

Sponsor
University of Alcala
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Raquel Lorenzo Moreno

physiotherapist

University of Alcala

Study Sites (1)

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