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Effectiveness of a Novel Device for Cervical Training in Cervicogenic Headache.

NCT05479149 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2023-01-27

No results posted yet for this study

Summary

The purpose of this study is to evaluate the clinical results in cervical spine range of motion, endurance deep cervical muscles, headache impact and physical activity enjoyment by a training protocol with the new device for cervical treatment (CDAT) versus conventional training protocol (CT) in subjects with cervicogenic headache.

Conditions

  • Cervicogenic Headache

Interventions

OTHER

Training protocol with the cervical device for treatment (CDAT).

Endurance training program of deep cervical flexors and deep cervical extensors with the cervical device for treatment.

OTHER

Conventional training protocol

Endurance training program of deep cervical flexors and deep cervical extensors with the conventional protocol.

Sponsors & Collaborators

  • Universitat Internacional de Catalunya

    lead OTHER

Principal Investigators

  • Pilar Pardos-Aguilella · UicCatalunya

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-08-05
Primary Completion
2022-10-15
Completion
2022-11-15

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05479149 on ClinicalTrials.gov