A Comparison of Seated Thoracic Manipulation and Targeted Supine Thoracic Manipulation on Cervical Flexion Motion and Pain
A Randomized Control Trial of the Immediate Effects of Seated Thoracic Manipulation and Targeted Supine Thoracic Manipulation on Cervical Spine Flexion Range of Motion and Pain
2 other identifiers
interventional
39
0 countries
N/A
Brief Summary
Thirty-nine patients with cervical spine pain were randomly assigned to either a seated thoracic manipulation or targeted supine thoracic manipulation group. Pain and flexion range of motion measures were taken before and after the intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Sep 2011
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2012
CompletedFirst Submitted
Initial submission to the registry
September 3, 2013
CompletedFirst Posted
Study publicly available on registry
September 10, 2013
CompletedSeptember 10, 2013
September 1, 2013
1.1 years
September 3, 2013
September 9, 2013
Conditions
Outcome Measures
Primary Outcomes (1)
neck pain
As measured by patient response at end range of flexion on a scale of 0 - 10.
pain measure taken immediately on first visit
Secondary Outcomes (1)
neck range of motion
range of motion assessed immediately in first visit
Study Arms (2)
seated general thoracic spine manipulation
EXPERIMENTALseated general thoracic spine manipulation
supine specific thoracic spine manipulation
EXPERIMENTALSpecific supine manipulation
Interventions
seated general thoracic spine manipulation
supine specific thoracic spine manipulation
Eligibility Criteria
You may not qualify if:
- identification of red flags suggestive of nonmusculoskeletal etiology, history of whiplash injury within six weeks of the initial visit, diagnosis of cervical spine stenosis, central nervous system involvement, or signs of nerve root compression (two of the following limited at the same level: strength, sensation, reflexes).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Chatham Universitylead
- Megan J. Olson Huntcollaborator
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
September 3, 2013
First Posted
September 10, 2013
Study Start
September 1, 2011
Primary Completion
October 1, 2012
Study Completion
October 1, 2012
Last Updated
September 10, 2013
Record last verified: 2013-09