- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04034186
The Quality of Physiotherapy in Low Back Pain Patients in Central Finland
The Assessment of the Content and Quality of Physiotherapy Management and Advice in Chronic Low-back Pain Patients in Central Finland
Chronic low back pain is one of the most common musculoskeletal disorders. In the Finnish Health 2000 survey the incidence of low back pain was 10% in men and 11% in women. Several evidence-based rehabilitation guidelines recommend exercise therapy treatment of chronic back pain. However, there are no studies in chronic low back pain patients concerning the assessment of the content and quality of exercise modalities adviced in clinical practise.
The aim of this study is to investigate the content and quality of physiotherapy management and advise in chronic low back pain patients in Central Finland.
Study Overview
Status
Conditions
Detailed Description
The participants in this study are 100 working-age unspecific low back pain patients from the Central Health Care District, who are referred for specialised care in the outpatient clinic in the Department of Physical Medicine and Rehabilitation in Central Finland Hospital. The participants will be asked to complete health-related questionnaires and an in-house made questionnaire of their back rehabilitation. The main questions are:
- The content about applied exercise modalities,
- How the progression of exercises have been advised?
- How pain was taken into account while exercising? The research will be carried out and coordinated by Central Finland Central Hospital, and the research project will take place between November 2014 and February 2019.
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- experiencing chronic low back pain,
- ability to communicate in Finnish language
Exclusion Criteria:
- previous back surgery in the preceding 12-month
- suspected or diagnosed lumbar disc herniation
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-constructed questionnaire; the content about instructed exercise modalities
Time Frame: During the physiotherapy treatment period
|
Strength training, aerobic exercise, aquatic exercise, mobility or something else
|
During the physiotherapy treatment period
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-constructed questionnaire; the way how the training was instructed by the physiotherapist
Time Frame: During the physiotherapy treatment period
|
Verbally, in written form or by practicing
|
During the physiotherapy treatment period
|
|
Self-constructed questionnaire; how back pain was taken into account in exercise guidance?
Time Frame: During the physiotherapy treatment period
|
Patient did not receive instructions on how pain should be taken into account while exercising, patient was urged to avoid exercises that caused pain while exercising, patient was urged to exercise within the limits of pain, patient was urged to practice despite the pain, some other instructions - what?
|
During the physiotherapy treatment period
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jari Ylinen, Docent, Chief physician in the Department of Physical Medicine and Rehabilitation, Central Finland Central Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Dnro 2E/2014
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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