Comparison of Different Massage Techniques Plus Conservative Applications in Low Back Pain
NCT ID: NCT02714803
Last Updated: 2016-03-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
61 participants
INTERVENTIONAL
2015-03-31
2015-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
FACTORIAL
TREATMENT
DOUBLE
Study Groups
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Connective tissue massage group
Connective tissue massage plus conservative applications including superficial thermal, electrotherapy and home exercise program were applied
"Connective tissue massage" and "Conservative applications"
Connective tissue massage and conservative aplications were applied 5 days per week for a total of 10 sessions for 2 weeks.
Classic massage group
Classic massage plus conservative applications including superficial thermal, electrotherapy and home exercise program were applied
"Classic massage group" and "Conservative applications"
Classic massage and conservative aplications were applied 5 days per week for a total of 10 sessions for 2 weeks.
Sham massage group
Sham massage plus conservative applications including superficial thermal, electrotherapy and home exercise program were applied
"Sham massage group" and "Conservative applications"
Sham massage and conservative aplications were applied 5 days per week for a total of 10 sessions for 2 weeks.
Interventions
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"Connective tissue massage" and "Conservative applications"
Connective tissue massage and conservative aplications were applied 5 days per week for a total of 10 sessions for 2 weeks.
"Classic massage group" and "Conservative applications"
Classic massage and conservative aplications were applied 5 days per week for a total of 10 sessions for 2 weeks.
"Sham massage group" and "Conservative applications"
Sham massage and conservative aplications were applied 5 days per week for a total of 10 sessions for 2 weeks.
Eligibility Criteria
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Inclusion Criteria
* Willing to participate
Exclusion Criteria
* neurological disease;
* psychiatric disease;
* serious chronic disease that could interfere with the outcomes (e.g., cardiovascular disease, epilepsy, rheumatoid arthritis),
* pregnant during the study
18 Years
65 Years
ALL
No
Sponsors
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Ataturk Training and Research Hospital
OTHER
Responsible Party
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Seyda TOPRAK CELENAY
Assistant Professor
Locations
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Ataturk Training and Research Hospital
Ankara, Cankaya, Turkey (Türkiye)
Countries
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Other Identifiers
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2015-11/33
Identifier Type: -
Identifier Source: org_study_id
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