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Spinal Manipulation Effectiveness in Spinal Disorders

Not Applicable
Conditions
Low Back Pain
Pain
Cervical Pain
Interventions
Other: Spinal Manipulation
Other: Sham manipulation
Registration Number
NCT03190187
Lead Sponsor
DAVID CRUZ DÍAZ
Brief Summary

The aim of the present intervention study is to determine the effectiveness of manipulation techniques.

Detailed Description

Spinal manipulation of the spine will be assessed in patients with musculoskeletal disorders to determine the effects of different manual therapy approaches.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
98
Inclusion Criteria
  • Currently suffering spinal related pain (neck, thoracic or lumbar).
  • Not receiving additional treatment for the treated condition.
Exclusion Criteria
  • Presence of red flags such as tumors or infection.
  • Recent surgery.
  • Fractures.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Spinal manipulationSpinal ManipulationSpinal manipulation to the spine will be applied to participants enrolled in this group.
Sham manipulationSham manipulationSham technique wich mimic the intervention manipulation with less force and different body location will be applied.
Primary Outcome Measures
NameTimeMethod
Visual analogical scaleChange from baseline to 4 weeks and 6 months of follow up.

Pain was measured using a visual analogical scale (VAS). The VAS consists of a 10-cm line, with the left extremity representing (absence of pain) and the right extremity indicating (the worse pain devisable). Participants were asked to indicate in the scale their current level of pain being higher values related with more intense pain

Secondary Outcome Measures
NameTimeMethod
Oswestry Disability IndexChange from baseline to 4 weeks and 6 months of follow up.

The Oswestry Disability Index is a 10 item questionnaire measuring low back pain related disability. Individual item scores range from 0 to 5. Scores on all items are summed and multiplied by 2 to provide a percentage ranging between 0 to 100 with higher scores indicating greater low back pain related disability.

Range of MotionChange from baseline to 4 weeks and 6 months of follow up.

The spinal range of motion will be assessed with a digital inclinometer which indicates the results in angular degrees.

Trial Locations

Locations (1)

University of Jaen

🇪🇸

Jaen, Spain

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