search
Back to results

"Examination of the Impact of a Dynamic Flexion Orthosis (Dynaflex®Ottobock) or of a Back Bandage (Lumbo Sensa®Ottobock) on the Voluntary Activation of the Back Muscles in Patients With Specific Back Pain"

Primary Purpose

Back Pain

Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Lumbo Sensa® bandage
Dynaflex® flexion orthosis
Sponsored by
RWTH Aachen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Back Pain

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

for the application with Dynaflex®:

  • central or foraminal lumbar stenosis, Claudicatio spinalis pathology
  • degenerative lumbar instability (e.g. Spondylolisthesis) with lumboischialgia or Claudicatio spinalis pathology
  • herniated vertebral disk with forms of ischialgia pain
  • age: 18-80 years

additionally for the application with LumboSensa®:

  • scoliosis
  • osteoporosis
  • inflammatory rheumatic back pain
  • Failed Back Surgery Syndrome
  • painful conditions after stabilizing or reinforcing surgeries

Exclusion Criteria:

  • paresis of the lower extremity
  • contact allergy to orthotic material
  • diseases in body regions with contact to orthosis, which become manifest neurologically/dermatologically
  • acute Spondylodiscitis
  • tumor diseases
  • recent vertebral body fractures
  • pregnant and lactating females
  • subject has been committed to an institution by legal or regulatory order
  • dependency or working relationship with the investigator
  • participation in a parallel interventional clinical study

Sites / Locations

  • Rehaklinik Schwertbad Aachen
  • Dept. of Rehabilitation- and Prevention Engineering, Institute of Applied Medical Engineering, Helmholtz Institute of RWTH Aachen University & Hospital
  • Spinal Surgery Center, Schön Klinik Nürnberg Fürth

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

No Intervention

No Intervention

Arm Label

Schwertbad Aachen

Schön Klinik Fürth

Schön Klinik Fürth & Schwertbad Aachen

RPE

Arm Description

20 Patients with specific back pain will get Lumbo Sensa® bandage. Study related procedures include a course with 6 exercises which shall be performed at the beginning and completion of the intervention: standing upright for 60s, keeping the upper body statically bent forward 40 degrees for 30s, carrying weight (1 kg) over a circular trajectory 3 times, stairs up and down for 60s, Chair rising test for 30s and 6 minutes walking test at the beginning and the end of the course. In addition, surface electromyogram (EMG) of the back muscles via surface electrodes during the course exercises will be recorded. Study procedures are the same for all study groups.

20 Patients with specific back pain will get Dynaflex® flexion orthosis. Study related procedures include a course with 6 exercises which shall be performed at the beginning and completion of the intervention: standing upright for 60s, keeping the upper body statically bent forward 40 degrees for 30s, carrying weight (1 kg) over a circular trajectory 3 times, stairs up and down for 60s, Chair rising test for 30s and 6 minutes walking test at the beginning and the end of the course. In addition, surface electromyogram (EMG) of the back muscles via surface electrodes during the course exercises will be recorded. Study procedures are the same for all study groups.

20 Patients with specific back pain will get no intervention. Study related procedures include a course with 6 exercises which shall be performed at the beginning and completion of the intervention: standing upright for 60s, keeping the upper body statically bent forward 40 degrees for 30s, carrying weight (1 kg) over a circular trajectory 3 times, stairs up and down for 60s, Chair rising test for 30s and 6 minutes walking test at the beginning and the end of the course. In addition, surface electromyogram (EMG) of the back muscles via surface electrodes during the course exercises will be recorded. Study procedures are the same for all study groups.

20 healthy Subjects of the same age without back pain participate in the course for one time to prove the significance of the procedures. (control group) Study related procedures include a course with 6 exercises: standing upright for 60s, keeping the upper body statically bent forward 40 degrees for 30s, carrying weight (1 kg) over a circular trajectory 3 times, stairs up and down for 60s, Chair rising test for 30s and 6 minutes walking test at the beginning and the end of the course. In addition, surface electromyogram (EMG) of the back muscles via surface electrodes during the course exercises will be recorded. Study procedures are the same for all study groups.

Outcomes

Primary Outcome Measures

change in activation of the lumbar muscles at everyday movements on targeted application of technical aids such as dynaflex® or LumboSensa® at 1 month assessed by questionnaires
questionnaires: EQ-5D™, ZCQ, VAS, OLBPDQ and questionnaire about intake of analgesics
change in activation of the lumbar muscles at everyday movements on targeted application of technical aids such as dynaflex® or LumboSensa® at 1 month assessed by course exercises
course: standing upright for 60s, keeping the upper body statically bent forward 40 degrees for 30s, carrying weight (1 kg) over a circular trajectory 3 times, stairs up and down for 60s, Chair rising test for 30s and 6 minutes walking test at the beginning and the end of the course

Secondary Outcome Measures

change in muscular activation due to specific back pain on surface EMG
surface electromyogram (EMG) of the back muscles via surface electrodes during the course exercises will be recorded
change in muscular activation regarding everyday life on EQ-5D™
EQ-5D™ (EuroQol-5 Dimension)
change in muscular activation regarding everyday life on ZCQ
Zürich Claudication Questionnaire (ZCQ)
change in muscular activation regarding everyday life on VAS
visual analog scale (VAS)
change in muscular activation regarding everyday life on OLBPDQ
Oswestry Low Back Pain Disability Questionnaire (OLBPDQ)
change in muscular activation regarding everyday life on questionnaire about intake of analgesics
change in muscular coordination of back muscles on a course with 6 exercises
course: standing upright for 60s, keeping the upper body statically bent forward 40 degrees for 30s, carrying weight (1 kg) over a circular trajectory 3 times, stairs up and down for 60s, Chair rising test for 30s and 6 minutes walking test at the beginning and the end of the course

Full Information

First Posted
August 11, 2015
Last Updated
August 26, 2015
Sponsor
RWTH Aachen University
Collaborators
Reha-Klinik Schwertbad, Schön Klinik Nürnberg Fürth
search

1. Study Identification

Unique Protocol Identification Number
NCT02536274
Brief Title
"Examination of the Impact of a Dynamic Flexion Orthosis (Dynaflex®Ottobock) or of a Back Bandage (Lumbo Sensa®Ottobock) on the Voluntary Activation of the Back Muscles in Patients With Specific Back Pain"
Official Title
"Examination of the Impact of a Dynamic Flexion Orthosis (Dynaflex®Ottobock) on the Voluntary Activation of the Back Muscles in Patients With Specific Low Back Pain" and "Examination of the Impact of a Back Bandage (Lumbo Sensa®Ottobock) on the Voluntary Activation of the Back Muscles in Patients With Specific Low Back Pain"
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Unknown status
Study Start Date
September 2015 (undefined)
Primary Completion Date
December 2016 (Anticipated)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
RWTH Aachen University
Collaborators
Reha-Klinik Schwertbad, Schön Klinik Nürnberg Fürth

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Aim of the study is to analyze systematically by using surface EMG the effect of the dynamic flexion orthosis Dynaflex® and the back bandage Lumbo Sensa® on the voluntary activation of the low back muscles and thereby on the muscles' stiffness. Patients have to pass a course with 6 different exercises in which they have to carry out certain activities of daily life under controlled conditions to examine, if the particular technical aid has a positive impact on pain-related activation of the back muscles.
Detailed Description
Usually low back pain is accompanied by male and prolonged activation of the back muscles through the Central Nervous System. It has been proved that this male innervation pattern are often related to a to the spine asymmetrical muscular activation. Biomechanically, both the asymmetric muscular activation as well as the prolonged activation of the muscles causes additional stress to the already damaged structures resulting in additional pain. Technical aids like back orthoses or bandages are supposed to relax the painful muscles and reduce pain in this way. However, no studies are available which analyze systematically the effect of such technical aids on the activation pattern of the back muscles. Aim of the study is to analyze systematically the effect of the dynamic flexion orthosis Dynaflex® and of the back bandage Lumbo Sensa® on the activation of the back muscles via surface EMG. On the one hand it shall be proven that the analyzed technical aids have an immediate impact on the activation of the back muscles which reduces the pain symptoms continuously. On the other hand it shall be demonstrated that surface EMG is a suitable approach to examine the effect of technical aids on the muscular activation of the back muscles focusing everyday situations or movements for the first time. From the results it shall be concluded on the everyday effect of orthosis or bandages for the discharge of the back muscles.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Back Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Schwertbad Aachen
Arm Type
Experimental
Arm Description
20 Patients with specific back pain will get Lumbo Sensa® bandage. Study related procedures include a course with 6 exercises which shall be performed at the beginning and completion of the intervention: standing upright for 60s, keeping the upper body statically bent forward 40 degrees for 30s, carrying weight (1 kg) over a circular trajectory 3 times, stairs up and down for 60s, Chair rising test for 30s and 6 minutes walking test at the beginning and the end of the course. In addition, surface electromyogram (EMG) of the back muscles via surface electrodes during the course exercises will be recorded. Study procedures are the same for all study groups.
Arm Title
Schön Klinik Fürth
Arm Type
Experimental
Arm Description
20 Patients with specific back pain will get Dynaflex® flexion orthosis. Study related procedures include a course with 6 exercises which shall be performed at the beginning and completion of the intervention: standing upright for 60s, keeping the upper body statically bent forward 40 degrees for 30s, carrying weight (1 kg) over a circular trajectory 3 times, stairs up and down for 60s, Chair rising test for 30s and 6 minutes walking test at the beginning and the end of the course. In addition, surface electromyogram (EMG) of the back muscles via surface electrodes during the course exercises will be recorded. Study procedures are the same for all study groups.
Arm Title
Schön Klinik Fürth & Schwertbad Aachen
Arm Type
No Intervention
Arm Description
20 Patients with specific back pain will get no intervention. Study related procedures include a course with 6 exercises which shall be performed at the beginning and completion of the intervention: standing upright for 60s, keeping the upper body statically bent forward 40 degrees for 30s, carrying weight (1 kg) over a circular trajectory 3 times, stairs up and down for 60s, Chair rising test for 30s and 6 minutes walking test at the beginning and the end of the course. In addition, surface electromyogram (EMG) of the back muscles via surface electrodes during the course exercises will be recorded. Study procedures are the same for all study groups.
Arm Title
RPE
Arm Type
No Intervention
Arm Description
20 healthy Subjects of the same age without back pain participate in the course for one time to prove the significance of the procedures. (control group) Study related procedures include a course with 6 exercises: standing upright for 60s, keeping the upper body statically bent forward 40 degrees for 30s, carrying weight (1 kg) over a circular trajectory 3 times, stairs up and down for 60s, Chair rising test for 30s and 6 minutes walking test at the beginning and the end of the course. In addition, surface electromyogram (EMG) of the back muscles via surface electrodes during the course exercises will be recorded. Study procedures are the same for all study groups.
Intervention Type
Device
Intervention Name(s)
Lumbo Sensa® bandage
Intervention Description
Patients have to wear it over 21-28 days for at least 8 hours a day
Intervention Type
Device
Intervention Name(s)
Dynaflex® flexion orthosis
Intervention Description
Patients have to wear it over 21-28 days for at least 8 hours a day
Primary Outcome Measure Information:
Title
change in activation of the lumbar muscles at everyday movements on targeted application of technical aids such as dynaflex® or LumboSensa® at 1 month assessed by questionnaires
Description
questionnaires: EQ-5D™, ZCQ, VAS, OLBPDQ and questionnaire about intake of analgesics
Time Frame
1 month
Title
change in activation of the lumbar muscles at everyday movements on targeted application of technical aids such as dynaflex® or LumboSensa® at 1 month assessed by course exercises
Description
course: standing upright for 60s, keeping the upper body statically bent forward 40 degrees for 30s, carrying weight (1 kg) over a circular trajectory 3 times, stairs up and down for 60s, Chair rising test for 30s and 6 minutes walking test at the beginning and the end of the course
Time Frame
1 month
Secondary Outcome Measure Information:
Title
change in muscular activation due to specific back pain on surface EMG
Description
surface electromyogram (EMG) of the back muscles via surface electrodes during the course exercises will be recorded
Time Frame
1 month
Title
change in muscular activation regarding everyday life on EQ-5D™
Description
EQ-5D™ (EuroQol-5 Dimension)
Time Frame
1 month
Title
change in muscular activation regarding everyday life on ZCQ
Description
Zürich Claudication Questionnaire (ZCQ)
Time Frame
1 month
Title
change in muscular activation regarding everyday life on VAS
Description
visual analog scale (VAS)
Time Frame
1 month
Title
change in muscular activation regarding everyday life on OLBPDQ
Description
Oswestry Low Back Pain Disability Questionnaire (OLBPDQ)
Time Frame
1 month
Title
change in muscular activation regarding everyday life on questionnaire about intake of analgesics
Time Frame
1 month
Title
change in muscular coordination of back muscles on a course with 6 exercises
Description
course: standing upright for 60s, keeping the upper body statically bent forward 40 degrees for 30s, carrying weight (1 kg) over a circular trajectory 3 times, stairs up and down for 60s, Chair rising test for 30s and 6 minutes walking test at the beginning and the end of the course
Time Frame
1 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: for the application with Dynaflex®: central or foraminal lumbar stenosis, Claudicatio spinalis pathology degenerative lumbar instability (e.g. Spondylolisthesis) with lumboischialgia or Claudicatio spinalis pathology herniated vertebral disk with forms of ischialgia pain age: 18-80 years additionally for the application with LumboSensa®: scoliosis osteoporosis inflammatory rheumatic back pain Failed Back Surgery Syndrome painful conditions after stabilizing or reinforcing surgeries Exclusion Criteria: paresis of the lower extremity contact allergy to orthotic material diseases in body regions with contact to orthosis, which become manifest neurologically/dermatologically acute Spondylodiscitis tumor diseases recent vertebral body fractures pregnant and lactating females subject has been committed to an institution by legal or regulatory order dependency or working relationship with the investigator participation in a parallel interventional clinical study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Catherine Disselhorst-Klug, Univ.-Prof. Dr. rer. nat.
Phone
+49 241 80 87011
Email
Disselhorst-klug@ame.rwth-aachen.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Catherine Disselhorst-Klug, Univ.-Prof. Dr. rer. nat.
Organizational Affiliation
Head: Dept. of Rehabilitation and Prevention Engineering, Institute of Applied Medical Engineering RWTH Aachen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rehaklinik Schwertbad Aachen
City
Aachen
ZIP/Postal Code
52066
Country
Germany
Facility Contact:
First Name & Middle Initial & Last Name & Degree
V Misch, Dr.med.
Phone
+49 241 6002 257
Email
v.misch@schwertbad.de
First Name & Middle Initial & Last Name & Degree
V Misch, Dr. med.
Facility Name
Dept. of Rehabilitation- and Prevention Engineering, Institute of Applied Medical Engineering, Helmholtz Institute of RWTH Aachen University & Hospital
City
Aachen
ZIP/Postal Code
52074
Country
Germany
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Catherine Disselhorst-Klug, Univ.-Prof. Dr.
First Name & Middle Initial & Last Name & Degree
L Igova
Facility Name
Spinal Surgery Center, Schön Klinik Nürnberg Fürth
City
Fürth
ZIP/Postal Code
90763
Country
Germany
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Klaus J. Schnake, Dr. med.
Phone
+49 911 9714 1700
Email
kschnake@schoen-kliniken.de
First Name & Middle Initial & Last Name & Degree
Klaus J. Schnake, Dr. med.

12. IPD Sharing Statement

Learn more about this trial

"Examination of the Impact of a Dynamic Flexion Orthosis (Dynaflex®Ottobock) or of a Back Bandage (Lumbo Sensa®Ottobock) on the Voluntary Activation of the Back Muscles in Patients With Specific Back Pain"

We'll reach out to this number within 24 hrs