Low Back PainNCT02861456
Feasibility of Using Functional Progression to Guide the Treatment of Adolescent Low Back Pain
A study testing Standard Model of Care and Alternative Model of Care in people with Low Back Pain and Spondylolysis, run by Nationwide Children's Hospital at 4 sites in United States.
Trial summary
The goal of the proposed research is to test the feasibility of a functional progression program to reduce cost and possible radiation exposure for adolescent athletes with low back pain. Read more about this study
- Who is it for?
- Ages 12 to 19 years
- Conditions the study is for
- Low Back Pain, Spondylolysis, Spondylolisthesis
- What is being tested?
- Standard Model of Care and Alternative Model of Care
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 16 participants
- Where
- 4 sitesUnited States
- Study dates
- Aug 2016to Aug 2018
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 12 to 19 years
- All sexes
- No healthy volunteers
- Child, Adult
Who may be able to join
- Age 12-19 years old
- Primary complaint of acute low back pain (<3months)
- Participates in some type of athletic activity on a regular basis (>2 times a week)
- Pain increases with lumbar extension
Who cannot join
- Advanced imaging performed already (MRI, SPECT, CT)
- Red flags present (bowel/bladder problems, saddle anesthesia, progressive neurological deficits, recent fever or infection, unexplained weight loss, unable to change symptoms with mechanical testing)
- Numbness and tingling in any lumbar dermatome
- Previous rest from sport >4 weeks without improved symptoms
- Other orthopedic injury or condition that would alter the plan of care for LBP (i.e. pregnancy, concomitant anterior cruciate ligament tear)
- History of lumbar surgery
Trial locations and contacts
4 sites in 1 country.
United States4 sites
Nationwide Children's Hospital Sports and Ortho PT East Broad
Columbus, Ohio, 43213
Nationwide Children's Hospital Sports and Ortho PT Dublin
Dublin, Ohio, 43017
Nationwide Children's Hospital Sports and Ortho PT New Albany
New Albany, Ohio, 43054
Nationwide Children's Hospital Sports and Orthopedic PT Westerville location
Westerville, Ohio, 43082
About this study
The goal of the proposed research is to test the feasibility of a functional progression program to reduce cost and possible radiation exposure for adolescent athletes with low back pain. Specifically the investigators plan to test the feasibility of using progression in rehabilitation to pragmatically differentially diagnose and treat adolescent athletes with low back pain, instead of using advanced imaging which is the current practice. The investigators propose to recruit 20 participants, with 10 of usual care (advanced imaging) and 10 of proposed intervention (functional progression) to assess the feasibility of using functional progress to guide treatment. The outcomes measured will be number of days for rest, time to start regular rehabilitation, pain experienced, functional outcomes, ability to return to sport, time needed to return to sport. If this pilot demonstrates the feasibility and a decreased rate of advanced imaging and similar clinical outcomes the investigators plan to progress this work into larger trials.
Read the detailed description
Low back pain (LBP) is a common complaint in adolescent athletes, with rates reported as high as 50% by the mid-teen years. Although low back pain in adolescent athletes may result from several different pathologies, spondylolysis--a fracture at the pars interarticularis--is the most common cause in this demographic, with a prevalence as high as 47%. The recommended treatment of spondylolysis and non-specific mechanical LBP is quite different. Patients with mechanical LBP are recommended to stay active, and perform rehabilitation if necessary, while the primary treatment for spondylolysis is rest for 3 months, physical therapy and bracing as needed. With the diagnosis of spondylolysis being fairly common in young athletes with low back pain, physicians need to have a high index of suspicion in making the diagnosis. Advanced imaging is often necessary to confidently rule in or out the diagnosis of spondylolysis. Advanced imaging increases diagnostic accuracy, but adds to the cost and potentially considerable radiation exposure. However, advanced imaging may not be necessary to effectively treat adolescents with low back pain.
Function, not imaging, is used to determine when a patient has healed from a spondylolytic injury. In fact, results of healing on imaging have no association with clinical outcome. Most defects do not heal with non-operative treatment suggesting that a successful clinical outcome does not depend on healing of the lesion. The functional progress that patients make is markedly different between patients with mechanical LBP and patients with a spondylolysis. The majority of adolescents with mechanical LBP can make a full functional recovery on their own or with a short period of rehabilitation. A patient with a spondylolytic injury may demonstrate an inability to make a full return to activity with rehabilitation and requires a period of rest from sport and high level activity to make a full functional recovery. Due to the differences in progression between mechanical LBP and spondylolysis, functional progress could be used to differentially diagnose these conditions. If effective, using functional progress instead of advanced imaging would be more cost-effective and expose the patient to significantly less radiation. In a retrospective review of adolescent patients presenting to the investigators sports medicine clinic with LBP, 80% had advanced imaging performed due to a concern of spondylolysis. Thirty-two percent of patients were positive for spondylolysis on advanced imaging, and 11% of patients had multiple advanced imaging performed due to lack of progress. No other significant findings were noted on advanced imaging. By using functional progress to determine the course of care, and only using advanced imaging when a patient does not respond to conservative care, there is the potential to significantly reduce the need for advanced imaging.
The primary risk of using functional progress in physical therapy (PT) instead of advanced imaging to determine to the course of care in adolescents with LBP is a delayed diagnosis for those who fail to respond to conservative care. The risk of missing a sinister pathology mimicking LBP can be minimized with a thorough clinical evaluation and radiographs if warranted. The results of the investigators' previous work demonstrate that early PT care in patients with a spondylolytic injury is safe and reduces time to return to sport. In a retrospective review with a cross-sectional follow-up, patients with an acute spondylolysis who began physical therapy as soon a 4 weeks (mean of 2 months) made a quicker functional recovery back to all activity and had similar clinical outcomes at 1-5 year follow-ups. A delayed diagnosis does not negatively impact long-term functional outcomes for patients with a spondylolysis as duration of symptoms is not found to be associated with outcome. Using logistic regression on the same dataset as above to determine factors associated with good short and long-term clinical outcomes, duration of symtpoms or time to diagnosis was not found to impact outcomes. On the other hand, delaying PT care to obtain advanced imaging is found to negatively impact outcomes in patients with mechanical LBP.
This project will lay the groundwork to demonstrate the feasibility of a functional progression to treat adolescent athletes with LBP. If successful, additional study will be proposed to test the effectiveness of intervention (functional progression) as compared to usual care (imaging) in improving the recovery outcome of LBP. Ultimately, this research would lead to change in the way adolescent athletes with LBP are treated, resulting in decreased cost, decreased exposure to radiation, and decreased time to begin rehabilitation. The results of this work would positively impact patients, clinicians, and decreased the costs to the health care system.
Control Cohort A series of 10 individuals who meet the inclusion criteria and are patients of the sports medicine physicians (Dr.s James MacDonald, Ravindran), physicians who are not recruiting patients for the experimental cohort but are still co-investigators, will serve as a non-randomized control cohort of typical clinical care and outcomes.
Description of the functional progression to guide treatment protocol. (Figure 1) Patients will be evaluated by their physician to determine appropriateness for participation in this study. Patients who meet the inclusion criteria and consent to participate in the pilot study as a part of the experimental cohort will not have advanced imaging done and will be referred directly to PT care for 2 times per week for 3 weeks. The functional progression protocol will be performed by physical therapists trained in the treatment and progression protocol. Patients will perform phase I of the PT protocol and progress to phase II as able without an increase in pain and with sufficiently proper mechanics. (Table 1) Patients will be assessed at each session to determine if they meet the criteria to begin the next step of functional PT progression back to sport. (Table 2) Those patients who meet these criteria within the designated 3 week period will progress into the next phase of functional PT for return to sport activity with an additional 2 weeks of PT. If these patients progress well in this third phase, and are able to meet the return to sport criteria, they will be discharged from PT and monitored by phone for recurrence of symptoms until 2 months. (Table 3) Those patients who do not progress through phase I or II functionally or without pain will be braced, as determined by their physician, and placed on rest from all activities excepting ADL's and their PT home exercise program and will be treated as patients with a presumed spondylolysis. Additionally, patients who are unable to meet the return to sport criteria within 5 weeks of PT will be braced, as deemed necessary by their physician, and placed on rest from all activities except ADL's and their PT home exercise program and will be treated as having a presumed spondylolysis. These patients will follow care appropriate for the condition. They will rest from sport until >2 months after initial evaluation , be braced as necessary, and ultimately complete 4 weeks of PT care to progress them as able back to sport activity. Patients who are treated as having a presumed spondylolysis will not be returned to sport before 3 months of rest as this period of rest has been found to produce optimal results.(El Rassi et al., 2013) Patients will have monthly re-evaluations with their physician until discharge. If at any point the patient is not responding as expected or the physician has concerns over the patient's safety, the physician can take the appropriate steps they feel are necessary for the safety of the patient. Patients who are classified as non-responders will be those who do not progress as expected for the typical course of mechanical LBP or spondylolysis.
Specific Outcome Variables
- Advanced imaging use during the episode of care: Computed tomography (CT), single-photon emission computed tomography (SPECT), and magnetic resonance imaging (MRI).
- Total cost will be calculated as the billed costs of physician visits, physical therapy visits, radiographs, advanced imaging, prescribed brace, and prescribed medication.
- Total number of PT visits will be calculated as the number of physical therapy visits completed for the LBP episode of care.
- The number of days from when the physician initially evaluates the patient and places them on hold from sport activity to when the patient was cleared to return to sport.
- , Clinical outcomes: Modified Odom's Criteria, and Micheli Functional Scale. Ability to return to sport This pilot study will not be randomized. All patients consenting to participate will be treated according to the treatment approach the co-investigating physicians have agreed to perform.
Blinding No blinding will be performed in this pilot trial as it is not feasible to blind either the clinicians or the patient to the treatment cohort.
Data Analysis Descriptive statistics of the patient demographics and outcome variables will be reported. The two treatment groups will be compared based on cost, imaging usage, and outcomes but will not perform statistical analysis due to the small sample size.
Treatment received Patient Characteristics (eg gender, age) Injury characteristics (eg duration of symptoms, type of symptoms Number of patients utilizing advanced imaging. Total cost of episode of care for LBP Total number of PT visits. Number of days to return to all sporting activity Clinical outcomes (eg pain, function, patient perceived improvement)
- Conditions
- Low Back Pain, Spondylolysis, Spondylolisthesis
- Being tested
- Standard Model of Care, Alternative Model of Care
- Keywords
- Adolescent, Low Back Pain, Athlete
- Medical subject headings
- Low Back Pain, Spondylolysis, Spondylolisthesis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Standard Model of CareOther
Alternative Model of CareOther
Also called Functional progression program
| Study group | Role | What they receive |
|---|---|---|
| Standard Care Group | Active comparator | Patient in the treatment arm will receive the Standard Model of Care as prescribed for their condition by their physician including but not limited to Advanced imaging, Rest, Bracing, Physical Therapy, and Medication. Receives: Other: Standard Model of Care |
| Functional Progression Group | Experimental | Patients who are randomized to the alternative model of care to guide treatment will not have advanced imaging done and will be referred directly to physical therapy care . If the patient is able to functional progress through phase I and II of physical therapy within 3 weeks and phase III within 5 weeks then they return to sport. If patient are unable to progress the are put on rest as a presumed vertebral injury (spondylolysis). Receives: Other: Alternative Model of Care |
What is being measured
The primary outcome is the main question the study is designed to answer.
Utilization of advanced imaging
Advanced imaging will be defined as anything beyond radiography (x-ray) used to diagnose patients low back pain
Measured: Approximately 3 months (Discharge from medical care (both physician and physical therapist))
Total cost of care
Total billed from hospital for the low back pain episode of care
Measured: Approximately 3 months (Discharge from medical care (both physician and physical therapist))
Secondary outcomes (3)
The number of days to return to all sporting activity.
The total number of days from when the patient begins the study to the date when they are released to return to sport by the health care provider
Measured: Approximately 3 months (Discharge from medical care (both physician and physical therapist))
Change in Numeric Pain Rating Scale
The Numeric Pain rating scale asks the patient their highest pain in the last 24 hours. The Numeric Pain Rating Scale is a 0-10 scale subjectively assessing a patients perceived level of pain. With 0 on the scale = to no pain, and 10 = to the worst pain imaginable.
Measured: Baseline, Approximately 3 months (Discharge from medical care (both physician and physical therapist))
Change in Micheli Functional Scale
The Micheli Functional Scale is a self-reported measure of functional ability and pain on a 0-100 scale with 0 being no disability and 100 representing maximum disability. This scale has been found to have validity and reliability in young athletes with LBP.
Measured: Baseline, Approximately 3 months (Discharge from medical care (both physician and physical therapist))
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Aug 2016 (estimated)
- Study startAug 2016
- Primary completionAug 2018
- Study completionAug 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (13)Papers the sponsor has linked to this study.
- Other trials for Low Back PainStudies of the same condition, open and under way.
- More trials run by Nationwide Children's HospitalThe sponsor's other registered studies.
- 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
- Health services research
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 16 participants (actual)
Sponsor and investigators
- Lead sponsor
- Nationwide Children's Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Mitchell Selhorst, Nationwide Children's Hospital
- Investigators
- Mitchell Selhorst, DPT, Principal investigator, Nationwide Children's Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02861456
- Sponsor's protocol ID
- IRB16-00032
- Status last verified
- Sep 2018
- First submitted
- 3 Aug 2016
- Last updated
- 2 Oct 2018
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No
Publications
Balague F, Dutoit G, Waldburger M. Low back pain in schoolchildren. An epidemiological study. Scand J Rehabil Med. 1988;20(4):175-9.
PubMed 2976526Burton AK, Clarke RD, McClune TD, Tillotson KM. The natural history of low back pain in adolescents. Spine (Phila Pa 1976). 1996 Oct 15;21(20):2323-8. doi: 10.1097/00007632-199610150-00004.
PubMed 8915066Ebrall PS. The epidemiology of male adolescent low back pain in a north suburban population of Melbourne, Australia. J Manipulative Physiol Ther. 1994 Sep;17(7):447-53.
PubMed 7989878Micheli LJ, Wood R. Back pain in young athletes. Significant differences from adults in causes and patterns. Arch Pediatr Adolesc Med. 1995 Jan;149(1):15-8. doi: 10.1001/archpedi.1995.02170130017004.
PubMed 7827653d'Hemecourt PA, Zurakowski D, d'Hemecourt CA, Curtis C, Ugrinow V, Deriu L, Micheli LJ. Validation of a new instrument for evaluating low back pain in the young athlete. Clin J Sport Med. 2012 May;22(3):244-8. doi: 10.1097/JSM.0b013e318249a3ce.
PubMed 22382433Miller R, Beck NA, Sampson NR, Zhu X, Flynn JM, Drummond D. Imaging modalities for low back pain in children: a review of spondyloysis and undiagnosed mechanical back pain. J Pediatr Orthop. 2013 Apr-May;33(3):282-8. doi: 10.1097/BPO.0b013e318287fffb.
PubMed 23482264El Rassi G, Takemitsu M, Glutting J, Shah SA. Effect of sports modification on clinical outcome in children and adolescent athletes with symptomatic lumbar spondylolysis. Am J Phys Med Rehabil. 2013 Dec;92(12):1070-4. doi: 10.1097/PHM.0b013e318296da7e.
PubMed 24141103Iwamoto J, Sato Y, Takeda T, Matsumoto H. Return to sports activity by athletes after treatment of spondylolysis. World J Orthop. 2010 Nov 18;1(1):26-30. doi: 10.5312/wjo.v1.i1.26.
PubMed 22474624Selhorst M, Fischer A, Graft K, Ravindran R, Peters E, Rodenberg R, Welder E, MacDonald J. Timing of Physical Therapy Referral in Adolescent Athletes With Acute Spondylolysis: A Retrospective Chart Review. Clin J Sport Med. 2017 May;27(3):296-301. doi: 10.1097/JSM.0000000000000334.
PubMed 27347866Klein G, Mehlman CT, McCarty M. Nonoperative treatment of spondylolysis and grade I spondylolisthesis in children and young adults: a meta-analysis of observational studies. J Pediatr Orthop. 2009 Mar;29(2):146-56. doi: 10.1097/BPO.0b013e3181977fc5.
PubMed 19352240Congeni J, McCulloch J, Swanson K. Lumbar spondylolysis. A study of natural progression in athletes. Am J Sports Med. 1997 Mar-Apr;25(2):248-53. doi: 10.1177/036354659702500220.
PubMed 9079183Iwamoto J, Takeda T, Wakano K. Returning athletes with severe low back pain and spondylolysis to original sporting activities with conservative treatment. Scand J Med Sci Sports. 2004 Dec;14(6):346-51. doi: 10.1111/j.1600-0838.2004.00379.x.
PubMed 15546329Childs JD, Fritz JM, Wu SS, Flynn TW, Wainner RS, Robertson EK, Kim FS, George SZ. Implications of early and guideline adherent physical therapy for low back pain on utilization and costs. BMC Health Serv Res. 2015 Apr 9;15:150. doi: 10.1186/s12913-015-0830-3.
PubMed 25880898
Study at a glance
From the registry record, last updated by the sponsor on 2 Oct 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Feasibility of Using Functional Progression to Guide the Treatment of Adolescent Low Back Pain
- ClinicalTrials.gov ID
- NCT02861456
- Acronym / sponsor ID
- IRB16-00032
- Conditions
- Low Back Pain, Spondylolysis, Spondylolisthesis
- Keywords
- Adolescent, Low Back Pain, Athlete
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 16 participants (actual)
- Lead sponsor
- Nationwide Children's HospitalUniversity, hospital or other
- Study start
- Aug 2016
- Primary completion
- Aug 2018 (actual)
- Study completion
- Aug 2018 (actual)
- First posted
- 10 Aug 2016 (estimated)
- 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 the proposed research is to test the feasibility of a functional progression program to reduce cost and possible radiation exposure for adolescent athletes with low back pain. Specifically the investigators plan to test the feasibility of using progression in rehabilitation to pragmatically differentially diagnose and treat adolescent athletes with low back pain, instead of using advanced imaging which is the current practice. The investigators propose to recruit 20 participants, with 10 of usual care (advanced imaging) and 10 of proposed intervention (functional progression) to assess the feasibility of using functional progress to guide treatment. The outcomes measured will be number of days for rest, time to start regular rehabilitation, pain experienced, functional outcomes, ability to return to sport, time needed to return to sport. If this pilot demonstrates the feasibility and a decreased rate of advanced imaging and similar clinical outcomes the investigators plan to progress this work into larger trials.
Detailed description
Low back pain (LBP) is a common complaint in adolescent athletes, with rates reported as high as 50% by the mid-teen years. Although low back pain in adolescent athletes may result from several different pathologies, spondylolysis--a fracture at the pars interarticularis--is the most common cause in this demographic, with a prevalence as high as 47%. The recommended treatment of spondylolysis and non-specific mechanical LBP is quite different. Patients with mechanical LBP are recommended to stay active, and perform rehabilitation if necessary, while the primary treatment for spondylolysis is rest for 3 months, physical therapy and bracing as needed. With the diagnosis of spondylolysis being fairly common in young athletes with low back pain, physicians need to have a high index of suspicion in making the diagnosis. Advanced imaging is often necessary to confidently rule in or out the diagnosis of spondylolysis. Advanced imaging increases diagnostic accuracy, but adds to the cost and potentially considerable radiation exposure. However, advanced imaging may not be necessary to effectively treat adolescents with low back pain.
Function, not imaging, is used to determine when a patient has healed from a spondylolytic injury. In fact, results of healing on imaging have no association with clinical outcome. Most defects do not heal with non-operative treatment suggesting that a successful clinical outcome does not depend on healing of the lesion. The functional progress that patients make is markedly different between patients with mechanical LBP and patients with a spondylolysis. The majority of adolescents with mechanical LBP can make a full functional recovery on their own or with a short period of rehabilitation. A patient with a spondylolytic injury may demonstrate an inability to make a full return to activity with rehabilitation and requires a period of rest from sport and high level activity to make a full functional recovery. Due to the differences in progression between mechanical LBP and spondylolysis, functional progress could be used to differentially diagnose these conditions. If effective, using functional progress instead of advanced imaging would be more cost-effective and expose the patient to significantly less radiation. In a retrospective review of adolescent patients presenting to the investigators sports medicine clinic with LBP, 80% had advanced imaging performed due to a concern of spondylolysis. Thirty-two percent of patients were positive for spondylolysis on advanced imaging, and 11% of patients had multiple advanced imaging performed due to lack of progress. No other significant findings were noted on advanced imaging. By using functional progress to determine the course of care, and only using advanced imaging when a patient does not respond to conservative care, there is the potential to significantly reduce the need for advanced imaging.
The primary risk of using functional progress in physical therapy (PT) instead of advanced imaging to determine to the course of care in adolescents with LBP is a delayed diagnosis for those who fail to respond to conservative care. The risk of missing a sinister pathology mimicking LBP can be minimized with a thorough clinical evaluation and radiographs if warranted. The results of the investigators' previous work demonstrate that early PT care in patients with a spondylolytic injury is safe and reduces time to return to sport. In a retrospective review with a cross-sectional follow-up, patients with an acute spondylolysis who began physical therapy as soon a 4 weeks (mean of 2 months) made a quicker functional recovery back to all activity and had similar clinical outcomes at 1-5 year follow-ups. A delayed diagnosis does not negatively impact long-term functional outcomes for patients with a spondylolysis as duration of symptoms is not found to be associated with outcome. Using logistic regression on the same dataset as above to determine factors associated with good short and long-term clinical outcomes, duration of symtpoms or time to diagnosis was not found to impact outcomes. On the other hand, delaying PT care to obtain advanced imaging is found to negatively impact outcomes in patients with mechanical LBP.
This project will lay the groundwork to demonstrate the feasibility of a functional progression to treat adolescent athletes with LBP. If successful, additional study will be proposed to test the effectiveness of intervention (functional progression) as compared to usual care (imaging) in improving the recovery outcome of LBP. Ultimately, this research would lead to change in the way adolescent athletes with LBP are treated, resulting in decreased cost, decreased exposure to radiation, and decreased time to begin rehabilitation. The results of this work would positively impact patients, clinicians, and decreased the costs to the health care system.
Control Cohort A series of 10 individuals who meet the inclusion criteria and are patients of the sports medicine physicians (Dr.s James MacDonald, Ravindran), physicians who are not recruiting patients for the experimental cohort but are still co-investigators, will serve as a non-randomized control cohort of typical clinical care and outcomes.
Description of the functional progression to guide treatment protocol. (Figure 1) Patients will be evaluated by their physician to determine appropriateness for participation in this study. Patients who meet the inclusion criteria and consent to participate in the pilot study as a part of the experimental cohort will not have advanced imaging done and will be referred directly to PT care for 2 times per week for 3 weeks. The functional progression protocol will be performed by physical therapists trained in the treatment and progression protocol. Patients will perform phase I of the PT protocol and progress to phase II as able without an increase in pain and with sufficiently proper mechanics. (Table 1) Patients will be assessed at each session to determine if they meet the criteria to begin the next step of functional PT progression back to sport. (Table 2) Those patients who meet these criteria within the designated 3 week period will progress into the next phase of functional PT for return to sport activity with an additional 2 weeks of PT. If these patients progress well in this third phase, and are able to meet the return to sport criteria, they will be discharged from PT and monitored by phone for recurrence of symptoms until 2 months. (Table 3) Those patients who do not progress through phase I or II functionally or without pain will be braced, as determined by their physician, and placed on rest from all activities excepting ADL's and their PT home exercise program and will be treated as patients with a presumed spondylolysis. Additionally, patients who are unable to meet the return to sport criteria within 5 weeks of PT will be braced, as deemed necessary by their physician, and placed on rest from all activities except ADL's and their PT home exercise program and will be treated as having a presumed spondylolysis. These patients will follow care appropriate for the condition. They will rest from sport until >2 months after initial evaluation , be braced as necessary, and ultimately complete 4 weeks of PT care to progress them as able back to sport activity. Patients who are treated as having a presumed spondylolysis will not be returned to sport before 3 months of rest as this period of rest has been found to produce optimal results.(El Rassi et al., 2013) Patients will have monthly re-evaluations with their physician until discharge. If at any point the patient is not responding as expected or the physician has concerns over the patient's safety, the physician can take the appropriate steps they feel are necessary for the safety of the patient. Patients who are classified as non-responders will be those who do not progress as expected for the typical course of mechanical LBP or spondylolysis.
Specific Outcome Variables
- Advanced imaging use during the episode of care: Computed tomography (CT), single-photon emission computed tomography (SPECT), and magnetic resonance imaging (MRI).
- Total cost will be calculated as the billed costs of physician visits, physical therapy visits, radiographs, advanced imaging, prescribed brace, and prescribed medication.
- Total number of PT visits will be calculated as the number of physical therapy visits completed for the LBP episode of care.
- The number of days from when the physician initially evaluates the patient and places them on hold from sport activity to when the patient was cleared to return to sport.
- , Clinical outcomes: Modified Odom's Criteria, and Micheli Functional Scale. Ability to return to sport This pilot study will not be randomized. All patients consenting to participate will be treated according to the treatment approach the co-investigating physicians have agreed to perform.
Blinding No blinding will be performed in this pilot trial as it is not feasible to blind either the clinicians or the patient to the treatment cohort.
Data Analysis Descriptive statistics of the patient demographics and outcome variables will be reported. The two treatment groups will be compared based on cost, imaging usage, and outcomes but will not perform statistical analysis due to the small sample size.
Treatment received Patient Characteristics (eg gender, age) Injury characteristics (eg duration of symptoms, type of symptoms Number of patients utilizing advanced imaging. Total cost of episode of care for LBP Total number of PT visits. Number of days to return to all sporting activity Clinical outcomes (eg pain, function, patient perceived improvement)
Study design
- Primary purpose
- Health services research
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Standard Care Group | Active comparator | Other: Standard Model of CarePatient in the treatment arm will receive the Standard Model of Care as prescribed for their condition by their physician including but not limited to Advanced imaging, Rest, Bracing, Physical Therapy, and Medication. |
| Functional Progression Group | Experimental | Other: Alternative Model of CarePatients who are randomized to the alternative model of care to guide treatment will not have advanced imaging done and will be referred directly to physical therapy care . If the patient is able to functional progress through phase I and II of physical therapy within 3 weeks and phase III within 5 weeks then they return to sport. If patient are unable to progress the are put on rest as a presumed vertebral injury (spondylolysis). |
Who may qualify
- Ages
- 12 to 19 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Key inclusion criteria (4 listed)
- Age 12-19 years old
- Primary complaint of acute low back pain (<3months)
- Participates in some type of athletic activity on a regular basis (>2 times a week)
- Pain increases with lumbar extension
Key exclusion criteria (6 listed)
- Advanced imaging performed already (MRI, SPECT, CT)
- Red flags present (bowel/bladder problems, saddle anesthesia, progressive neurological deficits, recent fever or infection, unexplained weight loss, unable to change symptoms with mechanical testing)
- Numbness and tingling in any lumbar dermatome
- Previous rest from sport >4 weeks without improved symptoms
- Other orthopedic injury or condition that would alter the plan of care for LBP (i.e. pregnancy, concomitant anterior cruciate ligament tear)
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 Model of Care | Other | Standard Care Group |
| Alternative Model of CareAlso: Functional progression program | Other | Functional Progression Group |
Primary outcome
Utilization of advanced imaging
Time frame: Approximately 3 months (Discharge from medical care (both physician and physical therapist))
Advanced imaging will be defined as anything beyond radiography (x-ray) used to diagnose patients low back pain
Total cost of care
Time frame: Approximately 3 months (Discharge from medical care (both physician and physical therapist))
Total billed from hospital for the low back pain episode of care
3 secondary outcomes
The number of days to return to all sporting activity.
Time frame: Approximately 3 months (Discharge from medical care (both physician and physical therapist))
Change in Numeric Pain Rating Scale
Time frame: Baseline, Approximately 3 months (Discharge from medical care (both physician and physical therapist))
Change in Micheli Functional Scale
Time frame: Baseline, Approximately 3 months (Discharge from medical care (both physician and physical therapist))
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Oct 2018.
- Background: PubMed 2976526Balague F, Dutoit G, Waldburger M. Low back pain in schoolchildren. An epidemiological study. Scand J Rehabil Med. 1988;20(4):175-9.
- Background: PubMed 8915066Burton AK, Clarke RD, McClune TD, Tillotson KM. The natural history of low back pain in adolescents. Spine (Phila Pa 1976). 1996 Oct 15;21(20):2323-8. doi: 10.1097/00007632-199610150-00004.
- Background: PubMed 7989878Ebrall PS. The epidemiology of male adolescent low back pain in a north suburban population of Melbourne, Australia. J Manipulative Physiol Ther. 1994 Sep;17(7):447-53.
- Background: PubMed 7827653Micheli LJ, Wood R. Back pain in young athletes. Significant differences from adults in causes and patterns. Arch Pediatr Adolesc Med. 1995 Jan;149(1):15-8. doi: 10.1001/archpedi.1995.02170130017004.
- Background: PubMed 22382433d'Hemecourt PA, Zurakowski D, d'Hemecourt CA, Curtis C, Ugrinow V, Deriu L, Micheli LJ. Validation of a new instrument for evaluating low back pain in the young athlete. Clin J Sport Med. 2012 May;22(3):244-8. doi: 10.1097/JSM.0b013e318249a3ce.
- Background: PubMed 23482264Miller R, Beck NA, Sampson NR, Zhu X, Flynn JM, Drummond D. Imaging modalities for low back pain in children: a review of spondyloysis and undiagnosed mechanical back pain. J Pediatr Orthop. 2013 Apr-May;33(3):282-8. doi: 10.1097/BPO.0b013e318287fffb.
- Background: PubMed 24141103El Rassi G, Takemitsu M, Glutting J, Shah SA. Effect of sports modification on clinical outcome in children and adolescent athletes with symptomatic lumbar spondylolysis. Am J Phys Med Rehabil. 2013 Dec;92(12):1070-4. doi: 10.1097/PHM.0b013e318296da7e.
- Background: PubMed 22474624Iwamoto J, Sato Y, Takeda T, Matsumoto H. Return to sports activity by athletes after treatment of spondylolysis. World J Orthop. 2010 Nov 18;1(1):26-30. doi: 10.5312/wjo.v1.i1.26.
- Background: PubMed 27347866Selhorst M, Fischer A, Graft K, Ravindran R, Peters E, Rodenberg R, Welder E, MacDonald J. Timing of Physical Therapy Referral in Adolescent Athletes With Acute Spondylolysis: A Retrospective Chart Review. Clin J Sport Med. 2017 May;27(3):296-301. doi: 10.1097/JSM.0000000000000334.
- Background: PubMed 19352240Klein G, Mehlman CT, McCarty M. Nonoperative treatment of spondylolysis and grade I spondylolisthesis in children and young adults: a meta-analysis of observational studies. J Pediatr Orthop. 2009 Mar;29(2):146-56. doi: 10.1097/BPO.0b013e3181977fc5.
- Background: PubMed 9079183Congeni J, McCulloch J, Swanson K. Lumbar spondylolysis. A study of natural progression in athletes. Am J Sports Med. 1997 Mar-Apr;25(2):248-53. doi: 10.1177/036354659702500220.
- Background: PubMed 15546329Iwamoto J, Takeda T, Wakano K. Returning athletes with severe low back pain and spondylolysis to original sporting activities with conservative treatment. Scand J Med Sci Sports. 2004 Dec;14(6):346-51. doi: 10.1111/j.1600-0838.2004.00379.x.
- Individual participant dataSharing planned: No
Related trials for Low Back Pain
Not yet recruiting
Effects of Hip Hinge Exercises on Pain, Range of Motion and Functional Disability in Non-specific Low Back Pain.
Low Back Pain
Not yet recruiting
Effect of Lumbar Stabilization Exercises With and Without YTWL (Scapular Stabilization Exercises) on Reducing Chronic Low Back Pain and Related Disability. A Randomized Clinical Trial,
Chronic Non Specific Mechanical Low Back Pain
Not yet recruiting
Comparing Non-Medicine Strategies for Improving Low Back Pain
Chronic Low-back Pain (cLBP), High-Impact Chronic Pain (HICP)
Not yet recruiting
Effects of Whole-Body Vibration and Cervical Stabilization With Core Stabilization in Young Adults With Non-Specific Low Back Pain
Nonspecific Low Back Pain
Not yet recruiting
Spinery Basivertebral Nerve Ablation for Vertebrogenic Chronic Low Back Pain
Low Back Pain, Chronic Low Back Pain (CLBP)
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. This study is not recruiting at the moment.
Mitchell Selhorst, DPT principal investigator
Nationwide Children's Hospital
4 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Standard Model of Care and Alternative Model of Care in people with Low Back Pain and Spondylolysis, run by Nationwide Children's Hospital at 4 sites 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 4 inclusion and 6 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: finished, as of the sponsor's last update on 2 Oct 2018. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 4 sites 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Utilization of advanced imaging (time frame: Approximately 3 months (Discharge from medical care (both physician and physical therapist))). The study lists 2 primary outcomes in all. 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 NCT02861456, which also lists 13 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 2 Oct 2018.