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Training Therapy for the Prevention of Back Pain

Primary Purpose

Back Pain, Lower Back Pain

Status
Completed
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
DAVID assisted training
training recommendation
Sponsored by
Medical University of Vienna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Back Pain

Eligibility Criteria

45 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • subjects must have suffered from (low) back pain for at least 6 days in the last month, without treatment by a doctor or feeling in need of treatment.
  • subject reported pain should reach the level of 3 or more on the numeric rating scale of 0-10 (0 equals no pain and 10 represents the strongest imaginable pain) [Larsen et al, 2008; Blagsted et al., 2008].
  • protocol documenting pain and work disability/limitations daily for a month must be completed
  • written consent after completed patient education by a physician must be given

Exclusion Criteria: (one or more of the following)

  • in order to rule out generalized musculoskeletal disorders, subjects should report discomfort or pain in no more than 3 different body parts
  • arterial hypertension and cardiovascular events such as myocardial infarction within the last year and / or cardiomyopathy NYHA III and IV.
  • symptomatic, lumbar disc herniation with associated neurological deficits
  • specific spinal diseases as potential underlying reason for a back pain syndrome including rheumatoid arthritis, ankylosing spondylitis, manifested osteoporosis with St.p. vertebral fractures, tumors.
  • St.p. traumatic damage of spine, pelvis or femur in the last 6 months
  • insufficiently healed surgical wounds in any body area
  • imminent musculoskeletal, spinal, hip or knee surgery
  • chronic infectious diseases
  • diagnosed mental illness
  • previous severe trauma with permanent Musculoskeletal dysfunction
  • pregnancy prior to study entrance examination
  • no written consent to the study
  • less than 1 year before retirement or planned job change within one year

Sites / Locations

  • University Department of Physical Medicine, Rehabilitation and Occupational Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

DAVID assisted training

training recommendation

Arm Description

Group I: Training assisted by DAVID devices

Group II: Training based on "stay active" recommendations

Outcomes

Primary Outcome Measures

Pain Frequency
Incidence of pain-days and pain-intensity

Secondary Outcome Measures

Sick-Leave
Days of sick-leave in total

Full Information

First Posted
January 3, 2018
Last Updated
October 19, 2020
Sponsor
Medical University of Vienna
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1. Study Identification

Unique Protocol Identification Number
NCT03393429
Brief Title
Training Therapy for the Prevention of Back Pain
Official Title
Training Therapy for the Secondary and Tertiary Prevention of Backache and Low Back Pain: A Randomized Controlled Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
November 1, 2017 (Actual)
Primary Completion Date
November 1, 2018 (Actual)
Study Completion Date
February 1, 2019 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Work place related (lower) back pain in medical personnel is limiting to workability. Even though occupational prevention programs are increasingly established, data on the effectiveness of training interventions offered at work-sites is largely missing. In this randomized, investigator-blind, controlled feasibility study we aim to compare the effectiveness of device assisted training therapy in comparison to a general recommendation "to stay active" or group gymnastics in terms of pain frequency and intensity (main outcome). Additional outcome variables are: quality of life, psychological well-being, work efficiency, of sick-leave days. Eligible employees (2 x 30) of the General Hospital of Vienna (AKH) over the age of 45 years suffering from (lower) back pain (>30 days/last year) of intensity ≥ 3 (numeric scale 0-10) will be included in two parallel groups. Group I starts with a device (DAVID) assisted training (40 training sessions; 2x / week) of the core trunk musculature. Group II gets instructions and an advice on how to "stay active" during the first 6 months. Assessment will be conducted before and after these 6 months; then groups are switched, thus, study subjects act as their own controls.
Detailed Description
Work place related pain syndromes of the (lower) back pose a major health problem for medical personnel. Beside the discomfort and limitations of the affected patients, a severe restriction of their ability to work must be considered. For secondary prevention of back pain, health promotion programs are recommended. These consist of psychosocial and ergonomic interventions and, above all, a regular strengthening of the stabilizing muscle groups. Specific strength and endurance training for the trunk musculature with appropriate equipment is considered as a useful preventive measure and thus commonly offered at large corporations, even during working hours of the staff. However, data clearly demonstrating the effectivity and cost-effectiveness of these interventions is largely missing. This pilot study serves several purposes: On one hand, the feasibility of a randomized, controlled study is to be examined, which is to prove the effectiveness of the medical training therapy in comparison to a general recommendation "to stay active" or in comparison to group gymnastics. In particular, logistical problems in the organization of training therapy and training compliance must be clarified. On the other hand, this pilot study serves to generate hypotheses. Several variables in regard to possible changes due to the training intervention will be investigated. Collected pilot data will be used for corresponding case number estimates of a subsequent confirmatory study. The outcome variables are: number of back pain days and intensity, quality of life, psychological well-being, work efficiency, days of sick-leave. Study Design Randomized, investigator-blind, controlled pilot study with parallel group comparison of outcomes in employees of the General Hospital of Vienna (AKH) over the age of 45 years Study Subjects 2 x 30 employees over the age of 45, who suffered more than 30 days of back and / or lower back pain of moderate to high intensity ≥ 3 (numeric scale 0-10) in the last year and suffer from pain in up to 3 body parts (in total) or less. Group I starts with a machine assisted training, group II starts after a period of observation half a year later. Study Interventions 40 training sessions (2x / week) with DAVID training machines, which aim to improve the strength, endurance and performance of the core trunk musculature. The training will be initiated after a sufficiently long period of adjustment to the guidelines of the American College of Sports Medicine. The training plan is created individually for each subject. 4 to 6 people per hour can work out simultaneously. The training should be completed in max 6 months or less. Group II gets instructions and an advice on how to "stay active" during the first 6 months. Assessment will be conducted before and after these 6 months. After 6 months the groups are switched (group I with the initial DAVID machine assisted training is left with recommendations to "stay active"; subjects from group II are now trained for 6 months by means of 40 training sessions (2x / week) with DAVID assistance), thus, study subjects act as their own controls.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
33 (Actual)

8. Arms, Groups, and Interventions

Arm Title
DAVID assisted training
Arm Type
Active Comparator
Arm Description
Group I: Training assisted by DAVID devices
Arm Title
training recommendation
Arm Type
Placebo Comparator
Arm Description
Group II: Training based on "stay active" recommendations
Intervention Type
Other
Intervention Name(s)
DAVID assisted training
Intervention Description
DAVID device assisted training under supervision
Intervention Type
Other
Intervention Name(s)
training recommendation
Intervention Description
training recommendation to "stay active"
Primary Outcome Measure Information:
Title
Pain Frequency
Description
Incidence of pain-days and pain-intensity
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Sick-Leave
Description
Days of sick-leave in total
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: subjects must have suffered from (low) back pain for at least 6 days in the last month, without treatment by a doctor or feeling in need of treatment. subject reported pain should reach the level of 3 or more on the numeric rating scale of 0-10 (0 equals no pain and 10 represents the strongest imaginable pain) [Larsen et al, 2008; Blagsted et al., 2008]. protocol documenting pain and work disability/limitations daily for a month must be completed written consent after completed patient education by a physician must be given Exclusion Criteria: (one or more of the following) in order to rule out generalized musculoskeletal disorders, subjects should report discomfort or pain in no more than 3 different body parts arterial hypertension and cardiovascular events such as myocardial infarction within the last year and / or cardiomyopathy NYHA III and IV. symptomatic, lumbar disc herniation with associated neurological deficits specific spinal diseases as potential underlying reason for a back pain syndrome including rheumatoid arthritis, ankylosing spondylitis, manifested osteoporosis with St.p. vertebral fractures, tumors. St.p. traumatic damage of spine, pelvis or femur in the last 6 months insufficiently healed surgical wounds in any body area imminent musculoskeletal, spinal, hip or knee surgery chronic infectious diseases diagnosed mental illness previous severe trauma with permanent Musculoskeletal dysfunction pregnancy prior to study entrance examination no written consent to the study less than 1 year before retirement or planned job change within one year
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gerold Ebenbichler, Prof. Dr.
Organizational Affiliation
University Department of Physical Medicine, Rehabilitation and Occupational Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Department of Physical Medicine, Rehabilitation and Occupational Medicine
City
Vienna
ZIP/Postal Code
1090
Country
Austria

12. IPD Sharing Statement

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