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Non-specific Back Pain and Spinal Manipulation

Predictors for Identifying Patients With Non-specific Back Pain Who Respond Favorably to Spinal Manipulation: a Prospective Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04388007
Enrollment
107
Registered
2020-05-14
Start date
2020-02-01
Completion date
2022-01-01
Last updated
2024-05-08

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

Conditions

Non-specific Back Pain

Keywords

Back pain, Spinal manipulation, Cohort study

Brief summary

The main purpose of this study is to identify short-term predictors of positive responses to a spinal manipulation treatment. To do this, positive responses to treatment, characterized by improvement in pain score, functional capacity, as well as the global perceived change will be evaluated using single and multiple logistic regressions in which biomechanical variables, comfort, expectation will used as potential predictors.

Detailed description

The main purpose of this study is to identify short-term predictors of positive responses to a spinal manipulation treatment. To do this, positive responses to treatment, characterized by improvement in pain score, functional capacity, as well as the global perceived change will be evaluated at baseline and at 7 days. Pain score will be also assessed every day with text-tracking. Global perceived change will be evaluated using single and multiple logistic regressions in which biomechanical variables, comfort, expectation will used as potential predictors. 100 individuals with a history of non-specific back pain will be recruited in a chiropractic care center.

Interventions

High velocity, low amplitude force manipulation

Sponsors

Université du Québec à Trois-Rivières
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Being aged over 18 years old * Presenting non-specific back pain (chronic \>=3 months or recurrent complaint) * Speaking French or English

Exclusion criteria

* Symptomatic thoracic pain * Non-musculoskeletal disorders pain * Pregnancy * Not eligible to spinal manipulation (if osteoporosis, vertebral fracture history, thoracic disk herniation)

Design outcomes

Primary

MeasureTime frameDescription
Thoracic Back Pain (Numerical Analog Scale)change from baseline to Day-7assessed by a 0-10 points scale, higher score means altered, lower score means improved
Functional Disability (Quebec Back Pain Disability Scale)change from baseline to Day-7assessed by 0-100 points questionary. Higher scores correlate to greater disability
Global Perceived Change Scaleat day-7assessed by a 11-point score scale: higher score means improved, lower score means altered

Secondary

MeasureTime frameDescription
Tampa Scale of Kinesiophobiaat baseline(pre-intervention)Questionary, Total score range from 17 to 68, Higher score indicate a worst outcome
Dosageduring the interventionassessed by a force-sensing table recording data through a computer software
Level of Comfortat baseline (post-intervention)Assessed with a 100mm scale : higher score means very comfortable
Level of anxietyat baseline (pre-intervention)Assessed using the State-Trait Anxiety Inventory (STAI) (score range from 20 (minimum) to 80 (maximum) : higher score mean a worst outcome)
Expectation (for improvement of pain and disability)at baseline (pre-intervention)assessed by a 11-point score scale : higher score means improved, lower score means altered
Socio-demographic factorsat baseline(pre-intervention)assessed with a patient history questionary

Countries

Canada

Outcome results

None listed

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