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Movement Control Exercises and Fascial Manipulation in Chronic Low Back Pain

Not Applicable
Conditions
Low Back Pain
Low Back Pain, Recurrent
Interventions
Other: FM and MCE
Other: FM and sham-MCE
Other: MCE and sham-FM
Other: Sham-MCE and sham-FM
Registration Number
NCT03270631
Lead Sponsor
Oulu University Hospital
Brief Summary

Subjects are recruited from the attendees of the multidisciplinary low back pain rehabilitation group before it takes place in University Hospital of Oulu at Physical and Rehabilitation Medicine (PRM) unit. Subjects were invited to participate by letter 2 weeks before the beginning of the rehabilitation. Subjects to rehabilitation are picked by doctor at PRM unit. The volunteered subjects are invited to the briefing of the study and those who are willing to participate, they filled in several questionnaires about pain, participation, disability and mood. After that the subjects are measured at baseline measurement. Subjects are randomized into the five groups. After the 3 months treatment and training the follow-up measurements are performed. Same questionnaires are filled in at that point as well. At 6 and 12 months the follow-up questionnaires (same as before) are sent to subjects.

Detailed Description

Subjects are recruited from the attendees of the multidisciplinary low back pain rehabilitation group before it takes place in University Hospital of Oulu at Physical and Rehabilitation Medicine (PRM) unit. Subjects were invited to participate by letter 2 weeks before the beginning of the rehabilitation. Subjects to rehabilitation are picked by doctor at PRM unit. The volunteered subjects are invited to the briefing of the study and those who are willing to participate, they filled in several questionnaires about pain, participation, disability and mood. After that the subjects are measured at baseline measurement. Subjects are randomized into the five groups: 1) control group, 2) fascial manipulation (FM) and movement control exercises (MCE), 3) sham-FM and MCE, 4) FM and sham-MCE and 5) sham-FM and sham-MCE. Physical therapists who perform treatments (FM), prescribing MCE and performing the measurements are blinded to each other. Physical therapist who is performing measurements is also blinded for the baseline measurements. There and 4 treatments of sham-FM, 4-5 treatments of FM, 4 treatments of sham-MCE and 4-6 treatments of MCE. Control group will receive only university hospital rehabilitation and will participate into the baseline and follow-up measurements. After the 3 months treatment and training the follow-up measurements are performed. Same questionnaires are filled in as at baseline. At 6 and 12 months the follow-up questionnaires (same as before) are sent to subjects.

Recruitment & Eligibility

Status
ENROLLING_BY_INVITATION
Sex
All
Target Recruitment
250
Inclusion Criteria
  • Chronic non-operatively treated low back pain or pain after the low back operation. Participation in multidisciplinary rehabilitation at University Hospital of Oulu.
Exclusion Criteria
  • Specific low back pain cause and earlier fascial manipulation treatment given.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
FM and MCEFM and MCESubjects will have 4-5 times of fascial manipulation (FM) treatment and 4-6 times movement control exercises (MCE) at home to be done based on movement control testing (MCT). Both are given in 3 month period.
FM and sham-MCEFM and sham-MCEFM 4-5 times in 3 months and 4 general exercise prescription.
MCE and sham-FMMCE and sham-FMSham-FM 4 times in 3 months including trigger point treatment in before decided points and 4-6 times MCE prescription and home exercises.
Sham-MCE and sham-FMSham-MCE and sham-FM4 general practice guiding and Sham-FM 4 times in 3 months including trigger point treatment in before decided points.
Primary Outcome Measures
NameTimeMethod
Change in Patient Specific Functional Scale (PSFS)Baseline, 3, 6 and 12 months

Three different meaningful tasks will be rated from 0 to 10 as how hard is the task.

Secondary Outcome Measures
NameTimeMethod
Change in Start backBaseline, 3, 6 and 12 months

Screening tool of the psychosocial risk factors

Change in Spinal mouseChange from baseline at 3 month

Mobility of the spine

Change in Tampa Scale of KinesiophobiaBaseline, 3, 6 and 12 months

Fear of movement

Change in Visual analogue ScaleBaseline, 3, 6 and 12 months

Pain scale

Change in Linton ÖrebroBaseline, 3, 6 and 12 months

Psychosocial risk factor

Change in PROMISBaseline, 3, 6 and 12 months

Quality of life

Change in Mobility of the hipsChange from baseline at 3 month

Hip ROM

Change in Lef-right discriminationChange from baseline at 3 month

How subject is able to understand right and left of the back

Change in Ultrasound of the fasciaChange from baseline at 3 month

Several fascial structures are measured

Change in OswestryBaseline, 3, 6 and 12 months

Disability index

Change in Movement control testsChange from baseline at 3 month

Clinical tests for LBP

Change in Balance measured with computerChange from baseline at 3 month

Power plate

Change in Two-point discriminationChange from baseline at 3 month

How far apart subject is able to feel two distinctive point of touch

Trial Locations

Locations (1)

University Hospital of Oulu

🇫🇮

Oulu, Finland

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