Skip to content

Thrust Manipulation Versus Non-Thrust Manipulation

Early Use of Thrust Manipulation Versus Non-Thrust Manipulation: A Randomized Clinical Trial

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01438203
Enrollment
149
Registered
2011-09-22
Start date
2011-02-28
Completion date
2012-02-29
Last updated
2012-09-05

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

Conditions

Mechanical Low Back Pain

Keywords

manipulation, mobilization, low back pain, treatment

Brief summary

The objective of this study is to investigate the comparative benefit of thrust and non-thrust manipulation on a population of patients with low back pain. The investigators hypothesize that there will be no difference in 4 week outcomes or greater, between the two groups.

Detailed description

Thrust manipulation is considered traditional spinal manipulation. Nonthrust manipulation is considered mobilization. The mobilization will be used in a similar manner as in clinical practice and this differs from past studies.

Interventions

Thrust manipulation is a passive procedure which involves a high velocity low amplitude thrust to the spinal region

Non-thrust manipulation involves a low amplitude, low speed mobilization to the targeted region while adjusting the procedure based on patient feedback

Sponsors

Walsh University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Patients, age 18 and older, with mechanically producible low back pain, who attend care at a physical therapy outpatient setting, will be screened for eligibility for the study. * For patients to meet inclusion requirements, they had to display a within session change in pain and/or range of motion during the assessment phase of the clinical examination. In other words, as the clinician performed their assessment and applied a passive accessory assessment technique, the pain and/or range of motion improved during that session, which suggests a favorable outcome using a comparable treatment technique. This is hallmark clinical finding in the patient response model and has been proposed as both a predictor of a positive outcome and as a prognostic variable toward long-term improvements in impairments.

Exclusion criteria

* The presence of any red flags (i.e., tumor, metabolic diseases, RA, osteoporosis, prolonged history of steroid use, etc.) * Signs consistent with nerve root compression (reproduction of low back or leg pain with straight leg raise at less than 45° * Muscle weakness involving a major muscle group of the lower extremity, * Diminished lower extremity muscle stretch reflex * Diminished or absent sensation to pinprick in any lower extremity dermatome) * Other

Design outcomes

Primary

MeasureTime frameDescription
Oswestry disability indexBaseline to discharge from therapy services (up to 4 months). An expected average is 4 weeks.Change score

Secondary

MeasureTime frameDescription
Numeric Pain Rating Scale (NPRS)Baseline to discharge from therapy services (up to 4 months). An expected average is 4 weeks.Change score

Countries

United States

Outcome results

None listed

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