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A Follow-up Comparison of Sensory Discrimination in Patients With Low Back Pain

A Follow-up Comparison of Sensory Discrimination in Patients With Low Back Pain: a Randomized Control Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03760887
Enrollment
102
Registered
2018-11-30
Start date
2018-06-01
Completion date
2018-12-30
Last updated
2019-04-23

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

Conditions

Low Back Pain

Keywords

Low back pain, Sensory, Tactile, Education

Brief summary

To determine if there is any carry over difference with sensation training to the low back for patients with low back pain with the addition of a training at home. This will be looked at to see if there is a difference in pain or back / leg movement right after the training and in a few days after doing some exercises at home.

Detailed description

In a previous case series patients with chronic Low Back Pain (LBP) who received tactile acuity training to their lower back in the absence of movement, experienced immediate positive changes in pain ratings and spinal movements. These changes, however, where only measured immediate post-intervention. This study aims to use a similar design of sensory discrimination for LBP, but will include a sensory discrimination home exercise program and compare groups at a follow-up visit for any difference between groups (48-96 hours) of the immediate changes. Changes will be assessed for pain and back and leg movement.

Interventions

After 5 minutes of sensory discrimination (using a 9 point grid) in the clinic patients will perform a home exercise program only

OTHERHome exercise program and home program of sensory discrimination

After 5 minutes of sensory discrimination (using a 9 point grid) in the clinic patients will perform a home exercise program and two 5 minutes sessions of sensory training at home each day.

Sponsors

St. Ambrose University
Lead SponsorOTHER

Study design

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

Masking description

Patients were randomly assigned to one of two groups (control or experimental).

Intervention model description

Randomized Control Trial

Eligibility

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

Inclusion criteria

* adults over the age of 18 * patients presenting at PT with a primary complaint of LBP * LBP being present for 3 months or more * fluent in English * willing to participate in the study * They also will need someone who can assist with a sensory discrimination HEP.

Exclusion criteria

* under age 18 * not able to read/understand the English language * prisoners * no medical issues precluding physical therapy treatment (red flags) * if they had undergone spinal surgery * if they had any skin or medical condition preventing them from receiving tactile stimuli on the lower back or had specific movement-based precautions, i.e., no active spinal flexion. - Patients presenting with leg pain only * Patients with neurological deficit only in the lower extremity

Design outcomes

Primary

MeasureTime frameDescription
Low Back Pain RatingChange from baseline to following treatment immediately upon completion of initial sessionNumeric Pain Rating Scale for Back pain (0 = no pain and 10 = worst pain)
Lumbar FlexionChange from baseline to treatment immediately upon completion of initial sessionActive trunk forward flexion measured in cm (finger tips to floor)
Straight Leg RaiseChange from baseline to treatment immediately upon completion of initial sessionNeurodynamic measurement of leg raise (lower limb tension test)

Countries

United States

Outcome results

None listed

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