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Clinical Trials/NCT02684916
NCT02684916
Completed
Not Applicable

Effectiveness of Chiropractic Manipulation Treatment Versus Placebo Manipulation on Children Aged 7-14 Years With Headache and Musculoskeletal Problems. A Randomized Clinical Trial

Nordic Institute of Chiropractic and Clinical Biomechanics1 site in 1 country200 target enrollmentOctober 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Headache
Sponsor
Nordic Institute of Chiropractic and Clinical Biomechanics
Enrollment
200
Locations
1
Primary Endpoint
Difference in number of days per week with headache over four months analyzed as repeated measures with end-point at four months.
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The primary aim of the study is to assess the effectiveness of chiropractic manipulation treatment versus placebo treatment in children suffering from headache for more than six months.

Detailed Description

The study is a two-armed parallel, randomized controlled clinical trial where children suffering from chronic headache and at the same time having one or more biomechanical dysfunctions of the spine are randomized to either chiropractic manipulation treatment or placebo manipulation treatment. The outcome is based on weekly sms responses collecting the number of days with headache the past week, intensity of headache and use of medication for headache. These are answered four weeks prior to initiation of treatment and 16 weeks thereafter. After the 16 weeks follow-up, a final questionnaire is completed including information about the course and the present headache status. The primary outcome is the number of days with headache. Secondary outcomes are intensity of headaches and use of medication for headache. Covariates are collected via baseline questionnaires on patient demographics; medical history; factors known to initiate, worsen or ease the headache; prevalence of headache in the nearest family; and behavioral patterns known to influence headache.

Registry
clinicaltrials.gov
Start Date
October 2015
End Date
October 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Nordic Institute of Chiropractic and Clinical Biomechanics
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Headaches for at least half a year.
  • Headache for at least 4 days pr. month.
  • At least one musculoskeletal dysfunction as identified by an experienced chiropractor as a movement restriction in one or more of the spinal joints and painful on manual palpation suitable for chiropractic manipulation treatment at the time of the initial screening.
  • Able to report information on headache via cell phone either by him- or herself or with help from the parents.

Exclusion Criteria

  • Contraindications for chiropractic treatment
  • Ongoing treatment for headache at another practitioner, except medical treatment 3 months prior to inclusion.
  • Lack of reporting baseline data via sms 4 weeks prior to inclusion.
  • Acute neck or head trauma during the trial period which is estimated to influence the headache

Outcomes

Primary Outcomes

Difference in number of days per week with headache over four months analyzed as repeated measures with end-point at four months.

Time Frame: Assessed weekly for a period of four months.

Patient or parent reported via sms-service.

Secondary Outcomes

  • Intensity of headache, graded on a 0-10 scale, where 10 is the worst, over four months analyzed as repeated measures with end-point at four months.(Assessed weekly for a period of four months.)
  • Use of medicine the past week due to headache over four months analyzed as repeated measures with end-point at four months.(Assessed weekly for a period of four months.)
  • Improvement on a seven point Likert scale (from 'totally recovered' to 'worse than ever') assessed at four months.(Assessed at the end of four months follow-up.)

Study Sites (1)

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