NCT04725279

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
67

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2019

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2019

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2019

Completed
1.5 years until next milestone

First Submitted

Initial submission to the registry

January 17, 2021

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 26, 2021

Completed
Last Updated

January 26, 2021

Status Verified

January 1, 2021

Enrollment Period

6 months

First QC Date

January 17, 2021

Last Update Submit

January 24, 2021

Conditions

Outcome Measures

Primary Outcomes (1)

  • 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.

    3 months passed between the first evaluation and the second.

Study Arms (1)

Type of rehabilitation treatment

EXPERIMENTAL

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.

Procedure: Rehabilitation Treatment: Physiotherapy, Electrotherapy or Exercises at home

Interventions

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.

Type of rehabilitation treatment

Eligibility Criteria

Age20 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Present vertigo of vestibular, neurological or cervical cause.
  • The last episode of vertigo occurred less than a year ago.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Facultad de Ciencias de la Salud

Zaragoza, 50009, Spain

Location

MeSH Terms

Interventions

Electric Stimulation Therapy

Intervention Hierarchy (Ancestors)

TherapeuticsPhysical Therapy ModalitiesRehabilitation

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

January 17, 2021

First Posted

January 26, 2021

Study Start

February 1, 2019

Primary Completion

July 31, 2019

Study Completion

July 31, 2019

Last Updated

January 26, 2021

Record last verified: 2021-01

Data Sharing

IPD Sharing
Will not share

Data from the 67 patients who were part of the study will not be shared with anyone who did not participate in the study.

Locations