Skip to main content
Clinical Trials/NCT02887638
NCT02887638
Completed
Not Applicable

Posture-related Headache: Profile Analysis and Intervention

Hasselt University5 sites in 2 countries36 target enrollmentJanuary 8, 2018
ConditionsHeadache

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Headache
Sponsor
Hasselt University
Enrollment
36
Locations
5
Primary Endpoint
Sitting-posture-profile
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Diagnosing and treating posture-related headache (PRH), such as tension-type and cervicogenic headache, is seriously hampered because of common features and complex interaction of the neurological and musculoskeletal system. Current therapies are therefore not as effective and the population of patients with PRH keeps on increasing. The diagnostic as well as the therapeutic process need more structure in order to select the most effective treatment; thereby contributing to preventive measures. This goal can be achieved through fundamental research with a clinically oriented background. Our study starts from a clinical problem, with a growing incidence, and is therefore highly relevant. Because sitting-posture seems to play an important role in PRH, the first step in the diagnostic process is to analyse postural differences between a PRH- and a control-group. In addition, the role of the dura mater in the headache-process will be examined. Patients with PRH will be classified in homogeneous groups based on these results. In a second phase individual-specific treatment programs will be composed. The general treatment-approach of postural abnormalities in the past failed because of the heterogeneous patient-populations. Sub-classifying musculoskeletal problems has been proven to be successful in the past (O'Sullivan & Dankaerts, non-specific low back pain).

Our study is divided in 2 phases:

  • phase 1: profile analysis (no intervention, experimental headache-group vs. asymptomatic controls)
  • phase 2: interventional phase (clustered headache-groups, based on the results of phase 1
Registry
clinicaltrials.gov
Start Date
January 8, 2018
End Date
May 18, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hasselt University
Responsible Party
Principal Investigator
Principal Investigator

prof. dr. Marita Granitzer

prof. dr.

Hasselt University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Sitting-posture-profile

Time Frame: week 1 up to week 8

Sitting-posture will be measured with a 3D-video analysis (Bonita, ©Vicon Motion Systems Ltd. UK). Markers are placed on specific anatomical reference points on the participant. Afterwards angles (°) will be automatically calculated (Nexus, ©Vicon Motion Systems Ltd. UK)

Pain-Profile

Time Frame: day 1

'Pain Pressure Threshold' will be measured. Through pressure- algometry (a) 'Pressure Pain Detection Threshold' (kPa/cm²) and (b) 'Pressure Pain Tolerance' (sec) will be determined (Somedic Sales AB, Stockholm Sweden).

Secondary Outcomes

  • Headache-related medication-use, headache intensity, duration and frequency.(week -4 up to week 8)
  • Impact of headache on the quality of life.(week -4 up to week 8)

Study Sites (5)

Loading locations...

Similar Trials