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Spinal Manipulation Effectiveness in Spinal Disorders

Spinal Manipulation Effectiveness in Pain, Disability and Range of Motion.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03190187
Enrollment
98
Registered
2017-06-16
Start date
2018-02-20
Completion date
2018-11-01
Last updated
2017-06-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Pain, Low Back Pain, Pain

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.

Interventions

OTHERSpinal Manipulation

Spinal manipulation based on orthopaedic manual therapy approach

OTHERSham manipulation

Patients will receive simulated spinal manipulation without force application

Sponsors

DAVID CRUZ DÍAZ
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Masking description

Patients will be randomly allocated to spinal manipulation group or sham group.

Intervention model description

Single blind parallel clinical trial

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
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

MeasureTime frameDescription
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.

Countries

Spain

Contacts

Primary ContactAntonio Amat, PhD
amamat@ujaen.es+34953212121
Backup ContactManuel Gonzalez, PhD
mgsanche@ujaen.es+3495312336

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026