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Effect of Cervical Traction on Balance in Cervical Radiculopathy Patients

Primary Purpose

Cervical Radiculopathy, Vertigo

Status
Completed
Phase
Not Applicable
Locations
Tunisia
Study Type
Interventional
Intervention
Cervical Traction Device
Sponsored by
University of Monastir
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cervical Radiculopathy focused on measuring Cervical Radiculopathy, Vertigo, Traction, Balance Postural

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Unilateral cervical radiculopathy of greater than three months

Exclusion Criteria:

  • History of surgery or bone-ligament damage to the cervical spine
  • Neurological and/or rheumatic diseases involving the cervical spine or which may result in impaired balance
  • Inner ear and vestibular pathology
  • Worsening of pain or intolerance in the manual cervical traction test

Sites / Locations

  • Physical Medicine and rehabilitation Department

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

Effective Traction/Sham Traction

Sham Traction/Effective Traction

Arm Description

Group of patients treated firstly with Effective Traction then with Sham Traction

Group of patients treated firstly with Sham Traction then with Effective Traction

Outcomes

Primary Outcome Measures

Change in static posturographic parameters: The center of pressure (CoP) movement: sway area
The CoP sway area (cm2) correspond to the the area which encloses the data points of the trajectory in relation with the body movement. The CoP sway area is assessed in two conditions (with open then closed eyes)
Change in static posturographic parameters: The CoP displacement amplitude
The CoP displacement amplitude (cm) in the anterior-posterior and medial-lateral trajectory correspond to the amount of body movement during a certain time interval in both trajectories. The CoP displacement amplitude is assessed in two conditions (with open then closed eyes)
Change in static posturographic parameters: The Cop velocity
The Cop velocity (cm/s) correspond to the velocity of movement of the body. The CoP velocity is assessed in two conditions (with open then closed eyes)
Change in static posturographic parameters: The Romberg quotient
The Romberg quotient correpond to the Ratio between Closed and Open Eyes Values of the previous parameters.
Change in static posturographic parameters: CoP position
The CoP position correspond to the location side in the frontal plan (left or right) and in the sagittal plan (anterior or posterior). The CoP position is assessed in two conditions (with open then closed eyes)

Secondary Outcome Measures

Change in pain intensity
The pain is assessed using a visual analog scale(VAS) /100 mm (minimum 0 mm and maximum 100 mm). The higher the score the worse the patient's pain.
Change in grip strength (Kg)
The grip strength is measured using Jamar Hydraulic Hand Dynamometer

Full Information

First Posted
September 30, 2020
Last Updated
July 17, 2021
Sponsor
University of Monastir
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1. Study Identification

Unique Protocol Identification Number
NCT04598113
Brief Title
Effect of Cervical Traction on Balance in Cervical Radiculopathy Patients
Official Title
The Immediate Effect of Cervical Traction on Balance in Cervical Radiculopathy Patients: A Randomized Cross-over Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
November 7, 2020 (Actual)
Primary Completion Date
March 13, 2021 (Actual)
Study Completion Date
March 20, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Monastir

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A cross-over randomized trial aiming to assess the immediate effect of cervical traction on balance disorders among patients with common cervical neuropathy. Authors hypothesized that as cervical traction alleviate radicular pain it may also improve patient balance disorders. Effective traction is compared to sham traction. Main outcome measures are balance parameters (force platform).
Detailed Description
A cross-over randomized trial was designed to assess the immediate effect of cervical intermittent traction on balance disorders among patients diagnosed with common cervical neuropathy. The diagnosis is confirmed or made by a physical medicine and rehabilitation physician with 15 Y of experience treating musculoskeletal disorders especially cervical neuropathy. Enrolled patients are randomly assigned to one of two arms (1 or 2). Patients in arm 1 (Effective Traction/Sham Traction) are treated firstly with effective traction than one week later with sham traction. Patients in arm 2 (Sham Traction/Effective Traction) are treated firstly with sham traction than one week later with effective traction. At baseline the epidemiological parameters, the pain intensity (VAS), the grip strength, the functional status (NDI), the psychological distress (HAD), the Brief Best Test and the balance parameters (force platform) are assessed. The pain intensity, the grip strength and the balance parameters are assessed before and immediately after cervical traction for comparison.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Radiculopathy, Vertigo
Keywords
Cervical Radiculopathy, Vertigo, Traction, Balance Postural

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Two interventions: Effective Traction (ET) and Sham Traction (ST) Two arms: Arm 1: Effective Traction/Sham Traction (ET than ST) and Arm 2: Sham Traction/Effective Traction (ST than ET) Wash out period = 1 week
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
The participant is treated with the same traction devise in the two interventions with just a traction intensity difference. The care provider who manipulate the traction device can't be blinded to allocation The investigator (performing balance tests) is blinded to the intervention type The outcome assessor is blinded to allocation
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Effective Traction/Sham Traction
Arm Type
Active Comparator
Arm Description
Group of patients treated firstly with Effective Traction then with Sham Traction
Arm Title
Sham Traction/Effective Traction
Arm Type
Sham Comparator
Arm Description
Group of patients treated firstly with Sham Traction then with Effective Traction
Intervention Type
Device
Intervention Name(s)
Cervical Traction Device
Intervention Description
While The patient is lie on the back his or her head is housed within the specific head portion of the device. The investigator inflate progressively the device using a valve and ensuring the patient's relaxation. The process of inflation is continued until the level of 12 Kg of pressure is reached. This maximum level of traction is maintained for 10 minutes then the process of deflation is started until the pressure decreased to 0 Kg. This maneuver is reproduced once again after 5 minutes of rest. The balance assessment using the force plate-from is done just before the intervention and 5 minutes after its end.
Primary Outcome Measure Information:
Title
Change in static posturographic parameters: The center of pressure (CoP) movement: sway area
Description
The CoP sway area (cm2) correspond to the the area which encloses the data points of the trajectory in relation with the body movement. The CoP sway area is assessed in two conditions (with open then closed eyes)
Time Frame
The CoP sway area assessment is done just before the intervention and 5 minutes after.
Title
Change in static posturographic parameters: The CoP displacement amplitude
Description
The CoP displacement amplitude (cm) in the anterior-posterior and medial-lateral trajectory correspond to the amount of body movement during a certain time interval in both trajectories. The CoP displacement amplitude is assessed in two conditions (with open then closed eyes)
Time Frame
The CoP displacement amplitude assessment is done just before the intervention and 5 minutes after.
Title
Change in static posturographic parameters: The Cop velocity
Description
The Cop velocity (cm/s) correspond to the velocity of movement of the body. The CoP velocity is assessed in two conditions (with open then closed eyes)
Time Frame
The Cop velocity assessment is done just before the intervention and 5 minutes after.
Title
Change in static posturographic parameters: The Romberg quotient
Description
The Romberg quotient correpond to the Ratio between Closed and Open Eyes Values of the previous parameters.
Time Frame
The Romberg quotient assessment is done just before the intervention and 5 minutes after.
Title
Change in static posturographic parameters: CoP position
Description
The CoP position correspond to the location side in the frontal plan (left or right) and in the sagittal plan (anterior or posterior). The CoP position is assessed in two conditions (with open then closed eyes)
Time Frame
The CoP position assessment is done just before the intervention and 5 minutes after.
Secondary Outcome Measure Information:
Title
Change in pain intensity
Description
The pain is assessed using a visual analog scale(VAS) /100 mm (minimum 0 mm and maximum 100 mm). The higher the score the worse the patient's pain.
Time Frame
The pain assessement is done just before the intervention and 5 minutes after
Title
Change in grip strength (Kg)
Description
The grip strength is measured using Jamar Hydraulic Hand Dynamometer
Time Frame
The measure is done just before the intervention and 5 minutes after
Other Pre-specified Outcome Measures:
Title
The Brief Best test
Description
Clinical test to assess the balance capacity during standing and walking.
Time Frame
The test is performed only once at baseline in each patient: before the Effective Traction in the Arm EffectiveTraction/ShamTraction and before the Sham Traction in the Arm ShamTraction/EffectiveTraction.
Title
Neck Disability Index (NDI)
Description
A self-administered questionnaire used to assess the self-rated disability. It contains 10 sections scored from 0 to 5 each. The total score range from 0 to 50. The higher the score the higher the patient's level of disability.
Time Frame
The questionnaire is administered only once at baseline in each patient: before the Effective Traction in the Arm EffectiveTraction/ShamTraction and before the Sham Traction in the Arm ShamTraction/EffectiveTraction.
Title
Hospital Anxiety and Depression scale
Description
A scale used to determine the level of anxiety and depression in patients. The questionnaire comprises seven questions for anxiety and seven questions for depression. Each response to a question is scored from 0 to 3. The total score for anxiety and depression separately range from 0 to 21. The higher the score the more sever the patient's anxiety and depression status.
Time Frame
The scale is administered only once at baseline in each patient: before the Effective Traction in the Arm EffectiveTraction/ShamTraction and before the Sham Traction in the Arm ShamTraction/EffectiveTraction.
Title
The short form (36) health survey: SF-36
Description
A questionnaire used to assess patient's health status (Quality of life). It yields an 8-scale profile of functional health and well-being scores: physical functioning (PF), role limitations due to physical problems (RP), bodily pain (BP), general health (GH), vitality (VT), social functioning (SF), role limitations due to emotional problems (RE), mental health (MH), and one single item scale on health transition. Score ranges from 0 to 100, with higher score indicating higher level of function and/or better health and lower score indicating lower level of function and/or bad health.
Time Frame
The questionnaire is administered only once at baseline in each patient: before the Effective Traction in the Arm EffectiveTraction/ShamTraction and before the Sham Traction in the Arm ShamTraction/EffectiveTraction.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Unilateral cervical radiculopathy of greater than three months Exclusion Criteria: History of surgery or bone-ligament damage to the cervical spine Neurological and/or rheumatic diseases involving the cervical spine or which may result in impaired balance Inner ear and vestibular pathology Worsening of pain or intolerance in the manual cervical traction test
Facility Information:
Facility Name
Physical Medicine and rehabilitation Department
City
Monastir
ZIP/Postal Code
5000
Country
Tunisia

12. IPD Sharing Statement

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Effect of Cervical Traction on Balance in Cervical Radiculopathy Patients

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