Chronic Low Back Pain (CLBP)NCT07719452
Lumbar Extension Strengthening in Addition to Manual Therapy and Exercise for Chronic Low Back Pain
A study testing Standard Physical Therapy and Lumbar Extensor Strengthening plus Standard Physical Therapy in people with Chronic Low Back Pain (CLBP), run by Brooke Army Medical Center at 1 site in United States.
Trial summary
The goal of this clinical trial is to determine the effect of adding lumbar strengthening exercises to a program of manual therapy and motor control exercises (standard therapy) in adults with chronic low back pain (cLBP). Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Chronic Low Back Pain (CLBP)
- What is being tested?
- Standard Physical Therapy and Lumbar Extensor Strengthening plus Standard Physical Therapy
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteUnited States
- Study dates
- 3 Aug 2026to 30 Jun 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Tricare Beneficiary
- 18-65 years old
- LBP ≥ 3 months without symptoms below the knee
- mODI ≥ 24%
- English speaking
- Available to actively take part in the study for 12 weeks
Who cannot join
- History of spine surgery or expecting spinal surgery
- Suspected or confirmed serious pathology (infection, cancer, fracture, cauda equina)
- Diagnosis of any vertebral fracture in the last 6 months
- Osteoporosis requiring pharmacologic treatment other than vitamin D, calcium supplements, or bisphosphonates
- History of any bone-related cancer or cancer that metastasized to the bone
- Diagnosed rheumatological or inflammatory disease
Show all 16Show fewer
- Progressive neurological disease
- Leg pain as the primary complaint (radiculopathy, peripheral vascular disease, stenosis)
- Contraindications to exercise and manual therapy
- Currently pregnant, self-reported or post-partum within the past 6 months
- Received physical therapy treatment for LBP in the past 6 months
- In the last 3 months, received injections, nerve ablation or blocks or is seeking such services
- Uncontrolled drug/alcohol addiction
- Currently under litigation related to cLBP
- Pending or expecting a Medical Evaluation Board (MEB)
- Retiring from the military within 18 months
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site
CPT Jennifer Moreno Primary Care Clinic - Physical Therapy
Fort Sam Houston, Texas, 78234
About this study
Official title: The Effect of Adding Lumbar Extension Strengthening to a Program of Manual Therapy & Motor Control Exercise in Individuals With Chronic Low Back Pain: A Randomized Control Trial
The goal of this clinical trial is to determine the effect of adding lumbar strengthening exercises to a program of manual therapy and motor control exercises (standard therapy) in adults with chronic low back pain (cLBP). Researchers will compare individuals with cLBP that receive lumbar extensor strengthening in addition to standard therapy compared to standard therapy alone to determine if there are differences in patient reported outcomes, lumbar multifidus thickness, low back endurance, and healthcare utilization between the groups.
All participants will engage in 8-weeks of physical therapy, receiving manual therapy and motor control exercises. Those in the intervention group will have additional low back strengthening exercises.
Read the detailed description
Purpose:
The purpose of this study is to determine the effect of adding lumbar strengthening exercises to a program of manual therapy and motor control exercises in individuals with chronic low back pain.
Primary Aim:
- Compare patient reported outcomes in individuals with cLBP that receive lumbar extensor strengthening in addition to a standard program of manual therapy \& motor control exercises compared to manual therapy \& motor control exercises alone.
Secondary Aims:
- Compare lumbar multifidus morphology (thickness) and extensor endurance in individuals with cLBP that receive lumbar extensor strengthening in addition to a standard program of manual therapy \& motor control exercises compared to manual therapy \& motor control exercises alone.
- Compare the amount and type of healthcare utilization between the two groups during the study period and the 12-month period following enrollment in the study.
Study Design:
This will be a parallel randomized control trial with two arms. Participants will be randomly assigned to either the experiment (manual therapy, motor control, \& lumbar strengthening) or control (manual therapy \& motor control) group.
Procedures:
The following procedures will be conducted once the participant has signed and received their Informed Consent Document (ICD) and HIPAA Authorization. The initial baseline visit involves the participant completing the electronic questionnaires, lumbar multifidus assessment (via ultrasound), back endurance test, randomization, and an initial physical therapy evaluation.
INITIAL VISIT - BASELINE MEASURES \& START OF TREATMENT
Baseline Questionnaires:
Participants will be provided a tablet to complete research questionnaires electronically, described below, using REDCap. If a tablet or the internet is not available, participants will fill out a paper copy that the research team will later transfer on to REDCap. REDCap is a secure, HIPAA-compliant web application used to build, administer, and record surveys.
Baseline Ultrasound Measurement - Lumbar Multifidus Thickness: Once the surveys have been completed, study participants will have their lumbar multifidus thickness measured. The subject will lie prone with a pillow underneath their pelvis. Ultrasound images, using a curvilinear probe, of the lumbar multifidus muscle at rest will be captured. Three measurements of the muscles thickness will be captured, and the average on each side will be recorded at two vertebral segments (L4/L5 \& L5/S1). Images will be saved on a facility device for measurement.
Baseline Back Endurance Performance: After completing the ultrasound measurements, subjects will perform a back endurance test (Biering-Sørensen test) on the variable angle roman chair. Subjects will be positioned prone at a 0 degree angle with their iliac crests at the edge of the hip pads and their legs stabilized on the ankle pads. The time starts once their trunk is horizontal with their hands crossed at the chest. The test will continue until the participant breaks from the horizontal posture.
Randomization:
Following completion of the above procedures, participants will be randomized into one of the following groups: the standard physical therapy group (SPT) consisting of manual therapy \& motor control exercises, or the experimental group consisting of the standard physical therapy protocol plus lumbar extensor strengthening exercises (SPT+LEX). The method of group assignment will be sequentially numbered opaque sealed envelopes. To minimize the risk of predicting the treatment assignment of the next eligible subject, randomization will be performed in permuted blocks of 2 or 4 with random variation of the blocking number.
Both groups will begin standard physical therapy treatment on the same day as their baseline examination and will be scheduled for their subsequent appointments at the Physical Therapy clinic. The initial physical therapy evaluation will last approximately 60 minutes.
The treatment groups are outlined below:
Group 1- Standard Physical Therapy (SPT):
Participants randomized to the SPT group (control group) will receive pragmatic treatments of manual therapy and motor control exercises based on their clinical presentation, which is consistent with standard patient care management of chronic lower back pain. They will attend a total of 10-14 visits over a course of 8 weeks, as is typical for routine care of individuals with cLBP. The treating physical therapist will use manual therapy and motor control exercise interventions that will be tailored to the patient's individual presentation. Manual therapy is used by physical therapists to improve and restore movement patterns of the spine and extremities in individuals with LBP. Examples of manual therapy interventions include joint mobilization or manipulation, manual muscle stretching, and soft-tissue mobilization. Motor control exercises (MCE) are designed to restore the coordination and timing of trunk musculature.
Group 2- Standard Physical Therapy Plus Lumbar Extensor Strengthening (SPT+LEX):
Participants randomized to the SPT+LEX group (experimental group) will receive the same pragmatic treatments of manual therapy and MCE as the SPT group over the same number of visits (10-14). In addition to MCE and manual therapy, this group will perform specific lumbar extensor strengthening (LEX) exercises toward the end of each physical therapy treatment visit. These LEX exercises target the lumbar extensor muscle group (to include the lumbar multifidus) and may be performed by lying prone on the edge of a bench or mat and lifting the legs to parallel while the torso is stabilized. Alternatively, they may be performed by stabilizing the hips and legs while lifting the torso to varying angles from horizontal with or without weights. LEX exercises are progressed by increasing hold times or weight, depending on the participant's tolerance and clinical progression
Total time spent with the participant will be equal in both groups (40 minutes)
- Conditions
- Chronic Low Back Pain (CLBP)
- Being tested
- Standard Physical Therapy, Lumbar Extensor Strengthening plus Standard Physical Therapy
- Keywords
- Physical Therapy, Manual Therapy, Motor Control Exercise, Lumbar Strengthening
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Standard Physical TherapyOther
Also called Manual Therapy, Motor Control Exercise
Participants randomized to the SPT group (control group) will receive pragmatic treatments of manual therapy and motor control exercises (MCE) based on their clinical presentation, which is consistent with standard patient care management of chronic lower back pain. They will attend a total of 10-14 visits over a course of 8 weeks, as is typical for routine care of individuals with cLBP. The treating physical therapist will use manual therapy and motor control exercise interventions that will be tailored to the patient's individual presentation.
Lumbar Extensor Strengthening plus Standard Physical TherapyOther
Participants randomized to the SPT+LEX group (experimental group) will receive the same pragmatic treatments of manual therapy and MCE as the control group over the same number of visits (10-14). In addition to MCE and manual therapy, this group will perform specific lumbar extensor strengthening. These exercises target the lumbar extensor muscle group (to include the lumbar multifidus) and may be performed by lying prone on the edge of a bench or mat and lifting the legs to parallel while the torso is stabilized. Alternatively, they may be performed by stabilizing the hips and legs while lifting the torso to varying angles from horizontal with or without weights.
| Study group | Role | What they receive |
|---|---|---|
| Standard Physical Therapy | Active comparator | Not described Receives: Other: Standard Physical Therapy |
| Standard Physical Therapy Plus Lumbar Extensor Strengthening | Experimental | Not described Receives: Other: Lumbar Extensor Strengthening plus Standard Physical Therapy |
What is being measured
The primary outcome is the main question the study is designed to answer.
Modified Oswestry Disability Index (mODI)
A 10-item disability questionnaire administered to evaluate the patient's symptoms and the functional impact of low back pain. Each item is scored on a 0-5 Likert scale. The total score is converted to a 0-100% disability index, with 0% indicating no functional limitation and 100% representing complete disability or a bedbound state.
Measured: Enrollment, 4, 8, 12, and 26-weeks
Secondary outcomes (6)
PROMIS-29
A 29-item self-reported questionnaire that assesses seven key health domains; physical function, pain interference, fatigue, sleep disturbance, depression, anxiety, social participation, plus a single item for pain intensity. Ratings are on a 1-5 Likert scale. The PROMIS-29 is a core outcome measure in chronic LBP research.
Measured: Enrollment, 4, 8, 12, and 26-weeks
Lumbar Spine Instability Questionnaire (LSIQ)
A 15-item self-reported questionnaire designed for patients with low back pain to assess perceived lumbar spinal instability. Items address symptom triggers, alleviating factors and movement-related behaviors. Higher scores reflect greater perceived instability.
Measured: Enrollment
Patient Acceptable Symptom State (PASS)
A dichotomous questionnaire to determine if the participant believes their symptoms are acceptable
Measured: Enrollment, 4, 8, 12, and 26-weeks
Healthcare Utilization
Participants will be queried on the healthcare resources they have used up to the time of taking this questionnaire. Items include other interventions, medication use, and specialty referrals
Measured: Enrollment, 4, 8, 12, 26-weeks
Lumbar Multifidus Thickness: L4-L5, L5-S1 bilaterally
Resting Lumbar Multifidus (LM) Thickness is a physical measure of muscle thickness of the lumbar multifidus. Measured in one plane, it is a surrogate measure for overall hypertrophy of the muscle. Thickness of the LM is measured in millimeters from the most posterior aspect of the facet joint to the thoracolumbar fascia.
Measured: Enrollment, 8, and 12-weeks
Back Endurance
The back endurance test (Biering-Sørensen test) will be conducted on a variable angle roman chair. Subjects will be positioned prone at a 0 degree angle with their iliac crests at the edge of the hip pads and their legs stabilized on the ankle pads. The time starts once their trunk is horizontal with their hands crossed at the chest. The test will continue until the participant breaks from the horizontal posture.
Measured: Enrollment, 8, and 12-weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Jul 2026
- Study start3 Aug 2026 (estimated)
- Primary completion30 Jun 2027 (estimated)
- Study completion30 Jun 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (6)Papers the sponsor has linked to this study.
- Other trials for Chronic Low Back Pain (CLBP)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Brooke Army Medical Center
- Sponsor type
- US federal agency
- Responsible party
- Principal investigator, Benjamin Campbell, Brooke Army Medical Center
- Investigators
- Benjamin Hando, PT, DSc, PhD, Study chair, Army-Baylor Doctoral Fellowship in Orthopedic Manual Physical Therapy
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07719452
- Sponsor's protocol ID
- C.2026.044d / eIRB #992009
- Status last verified
- Jun 2026
- First submitted
- 18 Jul 2026
- Last updated
- 22 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Zafereo J, Wang-Price S, Roddey T, Brizzolara K. Regional manual therapy and motor control exercise for chronic low back pain: a randomized clinical trial. J Man Manip Ther. 2018;26(4):193-202. doi:10.1080/10669817.2018.1433283
Dos Santos ECS, Dos Santos AT, da Silva NA, Carneiro SR, Rampazo EP, Magalhaes MO. Effectiveness of adding manual therapy to exercise for pain and disability in chronic non-specific low back pain: A systematic review and meta-analysis. Musculoskelet Sci Pract. 2026 Apr;82:103508. doi: 10.1016/j.msksp.2026.103508. Epub 2026 Jan 30.
PubMed 41643247Winder B, Keri PA, Weberg DE, Beneck GJ. Postural cueing increases multifidus activation during stabilization exercise in participants with chronic and recurrent low back pain: An electromyographic study. J Electromyogr Kinesiol. 2019 Jun;46:28-34. doi: 10.1016/j.jelekin.2019.03.005. Epub 2019 Mar 9.
PubMed 30878650Fortin M, Rye M, Roussac A, Montpetit C, Burdick J, Naghdi N, Rosenstein B, Bertrand C, Macedo LG, Elliott JM, Dover G, DeMont R, Weber MH, Pepin V. The Effects of Combined Motor Control and Isolated Extensor Strengthening versus General Exercise on Paraspinal Muscle Morphology, Composition, and Function in Patients with Chronic Low Back Pain: A Randomized Controlled Trial. J Clin Med. 2023 Sep 12;12(18):5920. doi: 10.3390/jcm12185920.
PubMed 37762861Cheng M, Xue Y, Cui M, Zeng X, Yang C, Ding F, Xie L. Global, Regional, and National Burden of Low Back Pain: Findings From the Global Burden of Disease Study 2021 and Projections to 2050. Spine (Phila Pa 1976). 2025 Apr 1;50(7):E128-E139. doi: 10.1097/BRS.0000000000005265. Epub 2025 Jan 22.
PubMed 39838749Cashin AG, Chou R, Weimer MB, McAuley JH. Low Back Pain: A Review. JAMA. 2026 Jul 14;336(2):144-158. doi: 10.1001/jama.2026.9631.
PubMed 42295944
Study at a glance
From the registry record, last updated by the sponsor on 22 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Adding Lumbar Extension Strengthening to a Program of Manual Therapy & Motor Control Exercise in Individuals With Chronic Low Back Pain: A Randomized Control Trial
- ClinicalTrials.gov ID
- NCT07719452
- Acronym / sponsor ID
- C.2026.044d / eIRB #992009
- Conditions
- Chronic Low Back Pain (CLBP)
- Keywords
- Physical Therapy, Manual Therapy, Motor Control Exercise, Lumbar Strengthening
- Study type
- Interventional
- Recruitment status
- Enrolling by invitation
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Brooke Army Medical CenterUS federal agency
- Study start
- 3 Aug 2026 (estimated)
- Primary completion
- 30 Jun 2027 (estimated)
- Study completion
- 30 Jun 2028 (estimated)
- First posted
- 22 Jul 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this clinical trial is to determine the effect of adding lumbar strengthening exercises to a program of manual therapy and motor control exercises (standard therapy) in adults with chronic low back pain (cLBP). Researchers will compare individuals with cLBP that receive lumbar extensor strengthening in addition to standard therapy compared to standard therapy alone to determine if there are differences in patient reported outcomes, lumbar multifidus thickness, low back endurance, and healthcare utilization between the groups.
All participants will engage in 8-weeks of physical therapy, receiving manual therapy and motor control exercises. Those in the intervention group will have additional low back strengthening exercises.
Detailed description
Purpose:
The purpose of this study is to determine the effect of adding lumbar strengthening exercises to a program of manual therapy and motor control exercises in individuals with chronic low back pain.
Primary Aim:
- Compare patient reported outcomes in individuals with cLBP that receive lumbar extensor strengthening in addition to a standard program of manual therapy \& motor control exercises compared to manual therapy \& motor control exercises alone.
Secondary Aims:
- Compare lumbar multifidus morphology (thickness) and extensor endurance in individuals with cLBP that receive lumbar extensor strengthening in addition to a standard program of manual therapy \& motor control exercises compared to manual therapy \& motor control exercises alone.
- Compare the amount and type of healthcare utilization between the two groups during the study period and the 12-month period following enrollment in the study.
Study Design:
This will be a parallel randomized control trial with two arms. Participants will be randomly assigned to either the experiment (manual therapy, motor control, \& lumbar strengthening) or control (manual therapy \& motor control) group.
Procedures:
The following procedures will be conducted once the participant has signed and received their Informed Consent Document (ICD) and HIPAA Authorization. The initial baseline visit involves the participant completing the electronic questionnaires, lumbar multifidus assessment (via ultrasound), back endurance test, randomization, and an initial physical therapy evaluation.
INITIAL VISIT - BASELINE MEASURES \& START OF TREATMENT
Baseline Questionnaires:
Participants will be provided a tablet to complete research questionnaires electronically, described below, using REDCap. If a tablet or the internet is not available, participants will fill out a paper copy that the research team will later transfer on to REDCap. REDCap is a secure, HIPAA-compliant web application used to build, administer, and record surveys.
Baseline Ultrasound Measurement - Lumbar Multifidus Thickness: Once the surveys have been completed, study participants will have their lumbar multifidus thickness measured. The subject will lie prone with a pillow underneath their pelvis. Ultrasound images, using a curvilinear probe, of the lumbar multifidus muscle at rest will be captured. Three measurements of the muscles thickness will be captured, and the average on each side will be recorded at two vertebral segments (L4/L5 \& L5/S1). Images will be saved on a facility device for measurement.
Baseline Back Endurance Performance: After completing the ultrasound measurements, subjects will perform a back endurance test (Biering-Sørensen test) on the variable angle roman chair. Subjects will be positioned prone at a 0 degree angle with their iliac crests at the edge of the hip pads and their legs stabilized on the ankle pads. The time starts once their trunk is horizontal with their hands crossed at the chest. The test will continue until the participant breaks from the horizontal posture.
Randomization:
Following completion of the above procedures, participants will be randomized into one of the following groups: the standard physical therapy group (SPT) consisting of manual therapy \& motor control exercises, or the experimental group consisting of the standard physical therapy protocol plus lumbar extensor strengthening exercises (SPT+LEX). The method of group assignment will be sequentially numbered opaque sealed envelopes. To minimize the risk of predicting the treatment assignment of the next eligible subject, randomization will be performed in permuted blocks of 2 or 4 with random variation of the blocking number.
Both groups will begin standard physical therapy treatment on the same day as their baseline examination and will be scheduled for their subsequent appointments at the Physical Therapy clinic. The initial physical therapy evaluation will last approximately 60 minutes.
The treatment groups are outlined below:
Group 1- Standard Physical Therapy (SPT):
Participants randomized to the SPT group (control group) will receive pragmatic treatments of manual therapy and motor control exercises based on their clinical presentation, which is consistent with standard patient care management of chronic lower back pain. They will attend a total of 10-14 visits over a course of 8 weeks, as is typical for routine care of individuals with cLBP. The treating physical therapist will use manual therapy and motor control exercise interventions that will be tailored to the patient's individual presentation. Manual therapy is used by physical therapists to improve and restore movement patterns of the spine and extremities in individuals with LBP. Examples of manual therapy interventions include joint mobilization or manipulation, manual muscle stretching, and soft-tissue mobilization. Motor control exercises (MCE) are designed to restore the coordination and timing of trunk musculature.
Group 2- Standard Physical Therapy Plus Lumbar Extensor Strengthening (SPT+LEX):
Participants randomized to the SPT+LEX group (experimental group) will receive the same pragmatic treatments of manual therapy and MCE as the SPT group over the same number of visits (10-14). In addition to MCE and manual therapy, this group will perform specific lumbar extensor strengthening (LEX) exercises toward the end of each physical therapy treatment visit. These LEX exercises target the lumbar extensor muscle group (to include the lumbar multifidus) and may be performed by lying prone on the edge of a bench or mat and lifting the legs to parallel while the torso is stabilized. Alternatively, they may be performed by stabilizing the hips and legs while lifting the torso to varying angles from horizontal with or without weights. LEX exercises are progressed by increasing hold times or weight, depending on the participant's tolerance and clinical progression
Total time spent with the participant will be equal in both groups (40 minutes)
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Standard Physical Therapy | Active comparator | Other: Standard Physical Therapy |
| Standard Physical Therapy Plus Lumbar Extensor Strengthening | Experimental | Other: Lumbar Extensor Strengthening plus Standard Physical Therapy |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Tricare Beneficiary
- 18-65 years old
- LBP ≥ 3 months without symptoms below the knee
- mODI ≥ 24%
- English speaking
Key exclusion criteria (16 listed)
- History of spine surgery or expecting spinal surgery
- Suspected or confirmed serious pathology (infection, cancer, fracture, cauda equina)
- Diagnosis of any vertebral fracture in the last 6 months
- Osteoporosis requiring pharmacologic treatment other than vitamin D, calcium supplements, or bisphosphonates
- History of any bone-related cancer or cancer that metastasized to the bone
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Standard Physical TherapyAlso: Manual Therapy, Motor Control ExerciseParticipants randomized to the SPT group (control group) will receive pragmatic treatments of manual therapy and motor control exercises (MCE) based on their clinical presentation, which is consistent with standard patient care management of chronic lower back pain. They will attend a total of 10-14 visits over a course of 8 weeks, as is typical for routine care of individuals with cLBP. The treating physical therapist will use manual therapy and motor control exercise interventions that will be tailored to the patient's individual presentation. | Other | Standard Physical Therapy |
| Lumbar Extensor Strengthening plus Standard Physical TherapyParticipants randomized to the SPT+LEX group (experimental group) will receive the same pragmatic treatments of manual therapy and MCE as the control group over the same number of visits (10-14). In addition to MCE and manual therapy, this group will perform specific lumbar extensor strengthening. These exercises target the lumbar extensor muscle group (to include the lumbar multifidus) and may be performed by lying prone on the edge of a bench or mat and lifting the legs to parallel while the torso is stabilized. Alternatively, they may be performed by stabilizing the hips and legs while lifting the torso to varying angles from horizontal with or without weights. | Other | Standard Physical Therapy Plus Lumbar Extensor Strengthening |
Primary outcome
Modified Oswestry Disability Index (mODI)
Time frame: Enrollment, 4, 8, 12, and 26-weeks
A 10-item disability questionnaire administered to evaluate the patient's symptoms and the functional impact of low back pain. Each item is scored on a 0-5 Likert scale. The total score is converted to a 0-100% disability index, with 0% indicating no functional limitation and 100% representing complete disability or a bedbound state.
6 secondary outcomes
PROMIS-29
Time frame: Enrollment, 4, 8, 12, and 26-weeks
Lumbar Spine Instability Questionnaire (LSIQ)
Time frame: Enrollment
Patient Acceptable Symptom State (PASS)
Time frame: Enrollment, 4, 8, 12, and 26-weeks
Healthcare Utilization
Time frame: Enrollment, 4, 8, 12, 26-weeks
Lumbar Multifidus Thickness: L4-L5, L5-S1 bilaterally
Time frame: Enrollment, 8, and 12-weeks
Back Endurance
Time frame: Enrollment, 8, and 12-weeks
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Jul 2026.
- BackgroundZafereo J, Wang-Price S, Roddey T, Brizzolara K. Regional manual therapy and motor control exercise for chronic low back pain: a randomized clinical trial. J Man Manip Ther. 2018;26(4):193-202. doi:10.1080/10669817.2018.1433283
- Background: PubMed 41643247Dos Santos ECS, Dos Santos AT, da Silva NA, Carneiro SR, Rampazo EP, Magalhaes MO. Effectiveness of adding manual therapy to exercise for pain and disability in chronic non-specific low back pain: A systematic review and meta-analysis. Musculoskelet Sci Pract. 2026 Apr;82:103508. doi: 10.1016/j.msksp.2026.103508. Epub 2026 Jan 30.
- Background: PubMed 30878650Winder B, Keri PA, Weberg DE, Beneck GJ. Postural cueing increases multifidus activation during stabilization exercise in participants with chronic and recurrent low back pain: An electromyographic study. J Electromyogr Kinesiol. 2019 Jun;46:28-34. doi: 10.1016/j.jelekin.2019.03.005. Epub 2019 Mar 9.
- Background: PubMed 37762861Fortin M, Rye M, Roussac A, Montpetit C, Burdick J, Naghdi N, Rosenstein B, Bertrand C, Macedo LG, Elliott JM, Dover G, DeMont R, Weber MH, Pepin V. The Effects of Combined Motor Control and Isolated Extensor Strengthening versus General Exercise on Paraspinal Muscle Morphology, Composition, and Function in Patients with Chronic Low Back Pain: A Randomized Controlled Trial. J Clin Med. 2023 Sep 12;12(18):5920. doi: 10.3390/jcm12185920.
- Background: PubMed 39838749Cheng M, Xue Y, Cui M, Zeng X, Yang C, Ding F, Xie L. Global, Regional, and National Burden of Low Back Pain: Findings From the Global Burden of Disease Study 2021 and Projections to 2050. Spine (Phila Pa 1976). 2025 Apr 1;50(7):E128-E139. doi: 10.1097/BRS.0000000000005265. Epub 2025 Jan 22.
- Background: PubMed 42295944Cashin AG, Chou R, Weimer MB, McAuley JH. Low Back Pain: A Review. JAMA. 2026 Jul 14;336(2):144-158. doi: 10.1001/jama.2026.9631.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Benjamin Hando, PT, DSc, PhD study chair
Army-Baylor Doctoral Fellowship in Orthopedic Manual Physical Therapy
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Standard Physical Therapy and Lumbar Extensor Strengthening plus Standard Physical Therapy in people with Chronic Low Back Pain (CLBP), run by Brooke Army Medical Center at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 16 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: enrolling by invitation, as of the sponsor's last update on 22 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Modified Oswestry Disability Index (mODI) (time frame: Enrollment, 4, 8, 12, and 26-weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07719452, which also lists 6 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jul 2026.