- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05784168
The Effect of Manual Therapy and Therapeutic Exercises on Pain and Functional Status in Persons With Low Back Pain
The Effect of Manual Therapy and Therapeutic Exercises on Pain and Functional Status in Persons With Chronic Non-specific Low Back Pain
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Kaunas, Lithuania
- Lithuanian Sports University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Non-specific low back pain (>8 weeks);
- Persons of working age;
- Must be able to perform therapeutic exercises.
Exclusion Criteria:
- Severe cardiovascular disease;
- Oncological disorders;
- Neurological symptoms of disorders;
- Osteoarthritis;
- Spondylolisthesis and spondylosis;
- Radiculopathy;
- Myelopathy;
- Spinal fracture.
- Pregnancy or lactation.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Manual therapy
6 weeks, 12 sessions in total, 2 times a week of manual therapy: spinal manipulation, specific mobilisations and stretches. Manual therapy treatments are carried out by a physiotherapist with more than 10 years of experience. In addition, 6 weeks, 5 times a week, a programme of therapeutic exercises at home: muscle strengthening and stretching, balance and coordination training, spinal stabilisation exercises. |
6 weeks, 12 sessions in total, 2 times a week of manual therapy: spinal manipulation, specific mobilisations and stretches. Manual therapy treatments are carried out by a physiotherapist with more than 10 years of experience. In addition, 6 weeks, 5 times a week, a programme of therapeutic exercises at home: muscle strengthening and stretching, balance and coordination training, spinal stabilisation exercises. |
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Experimental: Exercise therapy
6 weeks, 12 sessions in total, 2 times a week therapeutic exercise programme under the supervision of a physiotherapist. The exercise programme consisted of muscle strengthening and stretching, balance and coordination training, spinal stabilisation exercises. In addition, 6 weeks, 5 times a week, a programme of therapeutic exercises at home: muscle strengthening and stretching, balance and coordination training, spinal stabilisation exercises. |
6 weeks, 12 sessions in total, 2 times a week therapeutic exercise programme under the supervision of a physiotherapist. The exercise programme consisted of muscle strengthening and stretching, balance and coordination training, spinal stabilisation exercises. In addition, 6 weeks, 5 times a week, a programme of therapeutic exercises at home: muscle strengthening and stretching, balance and coordination training, spinal stabilisation exercises. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change from baseline Pain at 6 weeks
Time Frame: Baseline and after 6 weeks
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Pain was assessed using a Numerical Rating Scale (NRS) that used a 10-cm line with end-point descriptors such as 'no pain' marked at the left end and 'worst pain imaginable' marked at the right end.
Patients were asked to mark a point on the line that best represented their pain at the time of the evaluation.
The distance from 'no pain' to the patient's mark was then measured and recorded as the NRS score: 0 cm was defined as no pain, 1-3 cm as mild pain, 4 or 5 cm as moderate pain, 6-8 cm as severe pain and 9 or 10 cm as the worst pain imaginable.
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Baseline and after 6 weeks
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Change from baseline Oswestry Disability Index for functional status at 6 weeks
Time Frame: Baseline and after 6 weeks
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The Oswestry questionnaire (ODI) was used to assess the impact of back pain on functional status and disability.
It consists of ten questions (pain intensity, self-care, lifting objects, walking, sitting, standing, sleeping, sexual life, social life and travelling).
There are six answer options for each question, and the value of each question ranges from 0 (no problems/no disability) to 5 (major problems/major disability in this area).
The total ODI score is calculated as the sum of the scores for each question and the total ODI score ranges from 0 to 50.
The percentage of scores is calculated as follows: sum of scores / 50 x 100 = percentage (%).
The lower the score, the lower the impact of pain on functional status.
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Baseline and after 6 weeks
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Change from baseline Roland Morris Disability Questionnaire at 6 weeks
Time Frame: Baseline and after 6 weeks
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The Roland Morris Disability Questionnaire consists of 24 statements relating to daily living and physical activities such as personal care, sleep, work and walking.
The scale ranges from 0 to 24, with the highest score indicating maximum functional disability.
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Baseline and after 6 weeks
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Change from baseline Mobility of the lumbar spine at 6 weeks
Time Frame: Baseline and after 6 weeks
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The Schober test was used to assess lumbar spine mobility.
The test is performed with the subject standing upright, arms at the sides, and the examiner locates the midline between the iliac crests, on the dorsal side, and marks the first point there.
A second point is marked 10 cm above the first point.
5 cm below the first marked point, a third point shall be marked.
The subject is then asked to bend forward as far as he or she can without pain and without bending the knees, and the distance between the first and the third point is measured with a centimetre tape.
The test is negative if the distance between the marked points is 7 cm or more and positive if the distance is less than 7 cm, indicating limited mobility of the lumbar spine.
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Baseline and after 6 weeks
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Change from baseline Abdominal muscle static endurance at 6 weeks
Time Frame: Baseline and after 6 weeks
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Static abdominal muscle endurance test - Kraus-Weber.
The subject lies on the back, knees bent at 90 degrees, arms crossed over the chest.
The subject flexes the thorax, i.e. pulls the lower shoulder blade away from the surface, and is isometrically holds the body in this position.
The test is terminated if the subject remains in this position for more than 300 seconds.
The test shall be terminated when the lower scapular angle descends downwards and is no longer maintained or when the subject experiences unpleasant sensations and/or pain.
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Baseline and after 6 weeks
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Change from baseline Back muscle static endurance at 6 weeks
Time Frame: Baseline and after 6 weeks
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Static back muscle endurance test - Ito.
The subject lies on his/her stomach, arms at his/her sides, palms up.
The subject lifts the upper trunk to the lower sternum from the lying surface.
The test is terminated if the subject remains standing for more than 300 seconds.
If the subject does not maintain the position and touches the ground or experiences unpleasant sensations and/or pain, the test shall also be terminated.
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Baseline and after 6 weeks
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Change from baseline Kinesiophobia at 6 weeks
Time Frame: Baseline and after 6 weeks
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The Tampa Scale of Kinesiophobia was used to assess the fear of movement or repetitive trauma in pain patients.
The highest score indicates a high level of kinesiphobia.
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Baseline and after 6 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Vytautas Pilelis, Master, Lithuanian Sports University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- LithuanianSportsU12
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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