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Short Arc Multifidus Study

L

Logan College of Chiropractic

Status and phase

Unknown
Early Phase 1

Conditions

Multifidus Disuse Atrophy

Treatments

Procedure: Logan Short Arc Banding

Study type

Interventional

Funder types

Other

Identifiers

NCT00846664
396
SR0112080162

Details and patient eligibility

About

Patients will be performing Logan short arc banding protocols to see the effect on multifidus size

Full description

The subjects will initially be scanned by diagnostic ultrasound by to assess the cross sectional area of their lumbar multifidi. Then they will perform 3 sets of 30 second periods of Logan Short Arc Banding on the ATM machine twice a week for 4 weeks and then they will be scanned again using diagnostic ultrasound to assess the effects of the rehabilitation exercise.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 54 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male or Female ages 18-54

Exclusion criteria

  • Asymptomatic of: Low Back Pain, previous spinal injury, surgery or other condition affecting the spine, local infection, injury or malignancy; pregnancy or any condition affecting muscle reaction time.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Group 1
Experimental group
Description:
Group 1 wil perform short arc banding twice a week for four weeks and have diagnostic ultrasound of multifidus measured before and after intervention
Treatment:
Procedure: Logan Short Arc Banding

Trial contacts and locations

1

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Central trial contact

Adam Morrell, DC

Data sourced from clinicaltrials.gov

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