Usefulness of Rehabilitation in Patients With Cervical Imbalance
Primary Purpose
Rehabilitation, Cervical Vertigo
Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Rehabilitation Treatment: Physiotherapy, Electrotherapy or Exercises at home
Sponsored by
About this trial
This is an interventional diagnostic trial for Rehabilitation
Eligibility Criteria
Inclusion Criteria:
- Present vertigo of vestibular, neurological or cervical cause.
- The last episode of vertigo occurred less than a year ago.
Exclusion Criteria:
- Present acute musculoskeletal pathology in the lower limbs or lumbar spine.
- Present some lower limb amputation.
- Present unresolved visual pathology.
- Being active with anticancer treatment.
Sites / Locations
- Facultad de Ciencias de la Salud
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Type of rehabilitation treatment
Arm Description
Depending on whether the cervical pain associated with vertigo in the patients associated pain radiating to the arms or not, treatment with conventional physiotherapy or electrotherapy was prescribed. In addition, both groups had a control group that performed exercises at home prescribed by a physician.
Outcomes
Primary Outcome Measures
Number of patients who improve, worsen or do not present changes after rehabilitation treatment
It is evaluated whether the patients, after undergoing the corresponding prescribed rehabilitation treatment, are better, worse or the same as before undergoing it.
Secondary Outcome Measures
Full Information
NCT ID
NCT04725279
First Posted
January 17, 2021
Last Updated
January 24, 2021
Sponsor
Universidad de Zaragoza
1. Study Identification
Unique Protocol Identification Number
NCT04725279
Brief Title
Usefulness of Rehabilitation in Patients With Cervical Imbalance
Official Title
Usefulness of Rehabilitation in Patients With Cervical Imbalance. Use of Stabilometric Platform and Motion Sensors. (Provisional Title)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
February 1, 2019 (Actual)
Primary Completion Date
July 31, 2019 (Actual)
Study Completion Date
July 31, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad de Zaragoza
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Using the data obtained in a study carried out at the Hospital of Alcañiz (Teruel, Spain) between February and July 2019, with a stabilometric platform and with movement sensors, the investigators want to demonstrate that the rehabilitation works in those patients with vertigo or dizziness of cervical origin. For this, the data obtained from that sample, which was of 67 patients, will be analyzed in a pre-post rehabilitation treatment study, objectifying whether the patients improved or not, both in terms of imbalance and cervical pain, if any.
Detailed Description
Using the data obtained in a study carried out at the Hospital of Alcañiz (Teruel, Spain) between February and July 2019, with a stabilometric platform and with movement sensors, the investigators want to demonstrate that the rehabilitation works in those patients with vertigo or dizziness of cervical origin. For this, the data obtained from that sample, which was of 67 patients, will be analyzed in a pre-post rehabilitation treatment study, objectifying whether the patients improved or not, both in terms of imbalance and cervical pain, if any. The 67 patients attended the rehabilitation consultation where, after taking the anamnesis, they began to perform balance tests with a stabilometric platform and those patients with associated neck pain, with cervical motion sensors. Treatment with conventional physiotherapy, electrotherapy or exercises at home was prescribed as appropriate to each one. 3 months later, the patients were examined again in consultation, using a new anamnesis, the platform and the sensors. With the data obtained in said field work, carried out in 2019, the present study aims to analyze the usefulness of rehabilitation treatment in vertigo.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rehabilitation, Cervical Vertigo
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
67 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Type of rehabilitation treatment
Arm Type
Experimental
Arm Description
Depending on whether the cervical pain associated with vertigo in the patients associated pain radiating to the arms or not, treatment with conventional physiotherapy or electrotherapy was prescribed. In addition, both groups had a control group that performed exercises at home prescribed by a physician.
Intervention Type
Procedure
Intervention Name(s)
Rehabilitation Treatment: Physiotherapy, Electrotherapy or Exercises at home
Intervention Description
The 67 patients attended the rehabilitation consultation where, after taking the anamnesis, they began to perform balance tests with a stabilometric platform and those patients with associated neck pain, with cervical motion sensors. Treatment with conventional physiotherapy, electrotherapy or exercises at home was prescribed as appropriate to each one. 3 months later, the patients were examined again in consultation, using a new anamnesis, the platform and the sensors.
Primary Outcome Measure Information:
Title
Number of patients who improve, worsen or do not present changes after rehabilitation treatment
Description
It is evaluated whether the patients, after undergoing the corresponding prescribed rehabilitation treatment, are better, worse or the same as before undergoing it.
Time Frame
3 months passed between the first evaluation and the second.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Present vertigo of vestibular, neurological or cervical cause.
The last episode of vertigo occurred less than a year ago.
Exclusion Criteria:
Present acute musculoskeletal pathology in the lower limbs or lumbar spine.
Present some lower limb amputation.
Present unresolved visual pathology.
Being active with anticancer treatment.
Facility Information:
Facility Name
Facultad de Ciencias de la Salud
City
Zaragoza
ZIP/Postal Code
50009
Country
Spain
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Data from the 67 patients who were part of the study will not be shared with anyone who did not participate in the study.
Learn more about this trial
Usefulness of Rehabilitation in Patients With Cervical Imbalance
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