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Pilot Study on Digitally Supported Home Exercises for the Management of Unspecific Low Back Pain.

Primary Purpose

Low Back Pain

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Digitally supported home exercises
Sponsored by
University of Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Low Back Pain

Eligibility Criteria

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

Inclusion Criteria Group A and B

  • Patients with chronic unspecific low back pain
  • Patients of the Medical Training Therapy (MTT)
  • Adult male and female participant's (≥18 years)
  • Informed consent as documented by signature

Inclusion Criteria Group C and D

  • Participant reports unspecific low back pain
  • Receiving no therapy nor medical treatment for the last 6 months
  • Adult male and female participant's (≥18 years)
  • Informed consent as documented by signature

Exclusion criteria All Groups

  • Patients with specific causes for low back pain
  • Radicular syndrome
  • Unable to participate currently in the program due to pain
  • Pregnancy
  • Medication effecting postural balance
  • Uncorrected heavy visual impairment
  • Allergy to adhesive tape
  • Unable to understand and communicate in German or English

Sites / Locations

  • University Hospital Zurich, Directorate of Research and Education, Physiotherapy & Occupational Therapy Research

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

No Intervention

Experimental

No Intervention

Arm Label

Patients exercise

Patients control

Non-patients exercise

Non-patients control

Arm Description

Low back pain patients Next to basic medical physical training therapy group A receive a home exercising programme which involves 10 exercises for 2 minutes each with the Valedo training system.

Low back pain patients Group B will receive basic medical physical training therapy

non-patients Groups C will receive a home exercising programme which involves 10 exercises for 2 minutes each with the Valedo training system.

non-patients Group D will receive no intervention

Outcomes

Primary Outcome Measures

Postural Balance
Change of postural sway in anterior- posterior direction. Larger sway indicates worse balance. During each visit, 4 assessment repetitions of each 120 seconds are performed.

Secondary Outcome Measures

Motor Control
Lumbar spine and hip angles during task performance. Larger lumbar spine angles describe worse performance. Performance is assessed during a box lifting task and a waiter's bow task. At each assessment visit 5 repetitions of each task are performed.
Low back pain intensity
Numeric rating scale (0-10), 0 = no pain, 10 = worst imaginable pain
Disability
The Roland-Morris Disability Questionnaire (RMDQ) is used to assess disability. Scores range from 0 to 24, with a value of 24 indicating higher disability
Health quality of life
The short version of the World Health Organization Quality of Life Questionnaire (WOOQOL-BREF) is used to assess quality of Life. The scale has 4 subscales (raw scores range from 7 to 35, 6 to 30, 3 to 15 and 8 to 38). Larger values describe the better quality of life.
Fear of movement
The short version of the Tampa Scale for Kinesiophobia (TSK-11) Questionnaire is used to assess fear of movement. The TSK-11 scores range from 11 to 44, with higher scores describing higher fear of movement.
Fear of specific movements
Ratings of six movements (forward bending, backward bending, sideways bending, rotating, lifting a box, stretching upward) on each how painful or harmful a movement is and how careful a person is when executing the movement. Ratings range from 0 to 100. Large numbers indicate higher painfulness, fearfulness or caution when executing each movement.
Self-efficacy for managing chronic diseases
Self-efficacy for managing chronic disease 6-item scale (SES-6) Questionnaire. The mean scores are interpreted and are between 1 and 10. Higher values are the better outcome.

Full Information

First Posted
October 30, 2019
Last Updated
January 4, 2021
Sponsor
University of Zurich
Collaborators
ETH Zurich
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1. Study Identification

Unique Protocol Identification Number
NCT04364243
Brief Title
Pilot Study on Digitally Supported Home Exercises for the Management of Unspecific Low Back Pain.
Official Title
Pilot Study on Digitally Supported Home Exercises for the Management of Unspecific Low Back Pain.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
May 20, 2019 (Actual)
Primary Completion Date
October 23, 2020 (Actual)
Study Completion Date
October 23, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Zurich
Collaborators
ETH Zurich

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
The overall purpose of the study is to investigate effect of Digitally Supported Home Exercises (DSHE) in different groups for which digitally supported interventions could be beneficial. Balance is altered in individuals with low back pain and requires intervention Thus, the investigators will focus on the effect of DSHE to improve postural balance.
Detailed Description
The investigators want to investigate whether a digitally supported exercise program can improve the balance of people with non-specific lower back pain. During the exercise program, a computer game at home is controlled with the help of sensors attached to the body. Second aim is to record the daily activities of the participants and compare them with the back pain. The 120 participants in this study will be divided into four groups (A, B, C and D). In groups A and B 20 patients are included who are in treatment for chronic back pain and receive Medical Training Therapy (MTT). For groups C and D the investigators will invite each 40 participants who have back pain but are not in treatment for their back pain. Only participants in groups A and C receive the digitally supported home exercise program. Who gets the training program is randomized using stratified block randomization. The balance of all participants is measured four times. Between the 2nd and 3rd measurement the digitally supported exercise program is carried out. Between the 3rd and 4th assessement, participants in group A and C can exercise as much as they wish. The person who carries out the balance tests will not be informed which participant is in which group.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Model Description
2 x 2. Stratified randomization are used to assign patients to groups A and B and participants not receiving treatment to groups C and D. Participants are stratified by an average height.
Masking
Outcomes Assessor
Masking Description
Participants will be informed, instructed and provide consent to the study assistant, while assessments will be taken by a measurement assistant, blinded to the group assignment. Data which is not collected in all groups (e.g. intervention adherence) will be collected and managed by the study assistant.
Allocation
Randomized
Enrollment
38 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Patients exercise
Arm Type
Experimental
Arm Description
Low back pain patients Next to basic medical physical training therapy group A receive a home exercising programme which involves 10 exercises for 2 minutes each with the Valedo training system.
Arm Title
Patients control
Arm Type
No Intervention
Arm Description
Low back pain patients Group B will receive basic medical physical training therapy
Arm Title
Non-patients exercise
Arm Type
Experimental
Arm Description
non-patients Groups C will receive a home exercising programme which involves 10 exercises for 2 minutes each with the Valedo training system.
Arm Title
Non-patients control
Arm Type
No Intervention
Arm Description
non-patients Group D will receive no intervention
Intervention Type
Other
Intervention Name(s)
Digitally supported home exercises
Other Intervention Name(s)
Valedo home
Intervention Description
The training will comprise of 9 sessions (3 weekly) Each of the training sessions will last 20 minutes. This will result in a cumulative total intervention exercise time of 180 minutes.
Primary Outcome Measure Information:
Title
Postural Balance
Description
Change of postural sway in anterior- posterior direction. Larger sway indicates worse balance. During each visit, 4 assessment repetitions of each 120 seconds are performed.
Time Frame
At baseline (pretest 1), 3 weeks after pretest 1 (pretest 2), 3 weeks after pretest 2 (posttest 1), 6 weeks after posttest 1 (posttest2)
Secondary Outcome Measure Information:
Title
Motor Control
Description
Lumbar spine and hip angles during task performance. Larger lumbar spine angles describe worse performance. Performance is assessed during a box lifting task and a waiter's bow task. At each assessment visit 5 repetitions of each task are performed.
Time Frame
At baseline (pretest 1), 3 weeks after pretest 1 (pretest 2), 3 weeks after pretest 2 (posttest 1), 6 weeks after posttest 1 (posttest 2)
Title
Low back pain intensity
Description
Numeric rating scale (0-10), 0 = no pain, 10 = worst imaginable pain
Time Frame
At balseline (pretest 1), 3 weeks after pretest 1 (pretest 2), 3 weeks after pretest 2 (posttest 1), 6 weeks after posttest 1 (posttest 2)
Title
Disability
Description
The Roland-Morris Disability Questionnaire (RMDQ) is used to assess disability. Scores range from 0 to 24, with a value of 24 indicating higher disability
Time Frame
At baseline (pretest 1), 3 weeks after pretest 1 (pretest 2), 3 weeks after pretest 2 (posttest 1), 6 weeks after posttest 1 ( posttest 2)
Title
Health quality of life
Description
The short version of the World Health Organization Quality of Life Questionnaire (WOOQOL-BREF) is used to assess quality of Life. The scale has 4 subscales (raw scores range from 7 to 35, 6 to 30, 3 to 15 and 8 to 38). Larger values describe the better quality of life.
Time Frame
At baseline (pretest 1), 3 weeks after pretest 1 (pretest 2), 3 weeks after pretest 2 (posttest 1), 6 weeks after posttest 1 (posttest 2)
Title
Fear of movement
Description
The short version of the Tampa Scale for Kinesiophobia (TSK-11) Questionnaire is used to assess fear of movement. The TSK-11 scores range from 11 to 44, with higher scores describing higher fear of movement.
Time Frame
At baseline (pretest 1), 3 weeks after pretest 1 (pretest 2), 3 weeks after pretest 2 (posttest 1), 6 weeks after posttest 1 (posttest 2)
Title
Fear of specific movements
Description
Ratings of six movements (forward bending, backward bending, sideways bending, rotating, lifting a box, stretching upward) on each how painful or harmful a movement is and how careful a person is when executing the movement. Ratings range from 0 to 100. Large numbers indicate higher painfulness, fearfulness or caution when executing each movement.
Time Frame
At baseline (pretest 1), 3 weeks after pretest 1 (pretest 2), 3 weeks after pretest 2 (posttest 1), 6 weeks after posttest 1 (posttest 2)
Title
Self-efficacy for managing chronic diseases
Description
Self-efficacy for managing chronic disease 6-item scale (SES-6) Questionnaire. The mean scores are interpreted and are between 1 and 10. Higher values are the better outcome.
Time Frame
At baseline (pretest 1), 3 weeks after pretest 1 (pretest 2), 3 weeks after pretest 2 (posttest 1), 6 weeks after posttest 1 (posttest 2)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria Group A and B Patients with chronic unspecific low back pain Patients of the Medical Training Therapy (MTT) Adult male and female participant's (≥18 years) Informed consent as documented by signature Inclusion Criteria Group C and D Participant reports unspecific low back pain Receiving no therapy nor medical treatment for the last 6 months Adult male and female participant's (≥18 years) Informed consent as documented by signature Exclusion criteria All Groups Patients with specific causes for low back pain Radicular syndrome Unable to participate currently in the program due to pain Pregnancy Medication effecting postural balance Uncorrected heavy visual impairment Allergy to adhesive tape Unable to understand and communicate in German or English
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jaap Swanenburg, PhD
Organizational Affiliation
University of Zurich
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Zurich, Directorate of Research and Education, Physiotherapy & Occupational Therapy Research
City
Zurich
State/Province
ZH
ZIP/Postal Code
8091
Country
Switzerland

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Publication
Citations:
PubMed Identifier
35687390
Citation
Meinke A, Peters R, Knols RH, Swanenburg J, Karlen W. Feedback on Trunk Movements From an Electronic Game to Improve Postural Balance in People With Nonspecific Low Back Pain: Pilot Randomized Controlled Trial. JMIR Serious Games. 2022 Jun 10;10(2):e31685. doi: 10.2196/31685.
Results Reference
derived

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Pilot Study on Digitally Supported Home Exercises for the Management of Unspecific Low Back Pain.

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