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Università di PittsburghCervical Spine Focused Treatment for Patients With Persistent Concussion Symptoms and Neck Pain (ConCerv)
I dettagli dello studio clinico sono disponibili principalmente in inglese. Tuttavia, Trial Radar IA può essere d'aiuto! Basta cliccare su 'Spiega lo studio' per visualizzare e discutere le informazioni sullo studio nella lingua selezionata.
La sperimentazione clinica NCT06616272 (ConCerv) è uno studio interventistico per Commotio cerebrale, Dolore al Collo, attualmente in arruolamento. Avviato il 28 agosto 2025, prevede di arruolare 40 partecipanti. Sotto la guida di l'Università di Pittsburgh, dovrebbe concludersi entro il 15 dicembre 2025. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 12 novembre 2025.
Sommario breve
Assess the feasibility of recruiting, enrolling and randomizing patients with concussion symptoms and neck pain to receive manual therapy and cervical rehabilitative exercises in addition to standard concussion treatment.
In the usual care workflow provided at the participating concussion clinic, cervical spine rehab is not typically introduced until after week 4. The rationale is that neck pain is often a self-limiting condition that may resolve spontaneously, without the need for specific cervical spine rehab.
This study is chiefly focused on feasibility aims that revolve around developing changes to barriers in workflow issues at the participating concussion clinic, that would allow for earlier introduction of cervical spine rehab.
Descrizione dettagliata
This is a a single site pilot randomized controlled trial consisting of a total of 40 participants with concussion and neck pain, randomized to one of two groups (n=20 per group):
- early cervical spine focused treatment combined with standard concussion care.
- standard concussion care alone for 4 weeks, followed by delayed introduction (after 4 weeks) of cervical spine focused treatment (which is the usual care workflow at our clinical partner site.)
Both groups will receive the combination of cervical spine focused treatment and standard concussion care; the only variation being the timing of the introduction of the cervical spine care.
The primary endpoint will be 4 weeks from start of cervical rehabilitation intervention. The secondary would be the point of discharge. The duration of active participation in the study will be 8 weeks for the participants.
Titolo ufficiale
Cervical Spine Focused Treatment for Patients With Persistent Concussion Symptoms and Neck Pain: Pilot Study
Condizioni
Commotio cerebraleDolore al ColloPubblicazioni
Articoli scientifici e documenti di ricerca pubblicati su questo studio clinico:- Kontos AP, Elbin RJ, Trbovich A, Womble M, Said A, Sumrok VF, French J, Kegel N, Puskar A, Sherry N, Holland C, Collins M. Concussion Clinical Profiles Screening (CP Screen) Tool: Preliminary Evidence to Inform a Multidisciplinary Approach. Neurosurgery. 2020 Aug 1;87(2):348-356. doi: 10.1093/neuros/nyz545.
- Quatman-Yates CC, Hunter-Giordano A, Shimamura KK, Landel R, Alsalaheen BA, Hanke TA, McCulloch KL. Physical Therapy Evaluation and Treatment After Concussion/Mild Traumatic Brain Injury. J Orthop Sports Phys Ther. 2020 Apr;50(4):CPG1-CPG73. doi: 10.2519/jospt.2020.0301.
- McCrory P, Meeuwisse WH, Aubry M, Cantu B, Dvorak J, Echemendia RJ, Engebretsen L, Johnston K, Kutcher JS, Raftery M, Sills A, Benson BW, Davis GA, Ellenbogen RG, Guskiewicz K, Herring SA, Iverson GL, Jordan BD, Kissick J, McCrea M, McIntosh AS, Maddocks D, Makdissi M, Purcell L, Putukian M, Schneider K, Tator CH, Turner M. Consensus statement on concussion in sport: the 4th International Conference on Concussion in Sport held in Zurich, November 2012. Br J Sports Med. 2013 Apr;47(5):250-8. doi: 10.1136/bjsports-2013-092313. No abstract available.
- McCrory PR, Ariens T, Berkovic SF. The nature and duration of acute concussive symptoms in Australian football. Clin J Sport Med. 2000 Oct;10(4):235-8. doi: 10.1097/00042752-200010000-00002.
- Blanpied PR, Gross AR, Elliott JM, Devaney LL, Clewley D, Walton DM, Sparks C, Robertson EK. Neck Pain: Revision 2017. J Orthop Sports Phys Ther. 2017 Jul;47(7):A1-A83. doi: 10.2519/jospt.2017.0302.
- Hurwitz EL, Carragee EJ, van der Velde G, Carroll LJ, Nordin M, Guzman J, Peloso PM, Holm LW, Cote P, Hogg-Johnson S, Cassidy JD, Haldeman S; Bone and Joint Decade 2000-2010 Task Force on Neck Pain and Its Associated Disorders. Treatment of neck pain: noninvasive interventions: results of the Bone and Joint Decade 2000-2010 Task Force on Neck Pain and Its Associated Disorders. Spine (Phila Pa 1976). 2008 Feb 15;33(4 Suppl):S123-52. doi: 10.1097/BRS.0b013e3181644b1d.
- Reid SA, Rivett DA, Katekar MG, Callister R. Sustained natural apophyseal glides (SNAGs) are an effective treatment for cervicogenic dizziness. Man Ther. 2008 Aug;13(4):357-66. doi: 10.1016/j.math.2007.03.006. Epub 2007 Oct 22.
- van der Walt K, Tyson A, Kennedy E. How often is neck and vestibulo-ocular physiotherapy treatment recommended in people with persistent post-concussion symptoms? A retrospective analysis. Musculoskelet Sci Pract. 2019 Feb;39:130-135. doi: 10.1016/j.msksp.2018.12.004. Epub 2018 Dec 11.
- Jones C, Sterling M. Clinimetrics: Neck Disability Index. J Physiother. 2021 Apr;67(2):144. doi: 10.1016/j.jphys.2020.09.001. Epub 2021 Mar 19. No abstract available.
- Cleland JA, Childs JD, Whitman JM. Psychometric properties of the Neck Disability Index and Numeric Pain Rating Scale in patients with mechanical neck pain. Arch Phys Med Rehabil. 2008 Jan;89(1):69-74. doi: 10.1016/j.apmr.2007.08.126.
Altri ID dello studio
- ConCerv
- STUDY24040157
Numero NCT
Data di inizio (effettiva)
2025-08-28
Ultimo aggiornamento pubblicato
2025-11-12
Data di completamento (stimata)
2025-12-15
Arruolamento (previsto)
40
Tipo di studio
Interventistico
FASE
N.D.
Stato
In arruolamento
Parole chiave
concussion care
cervical rehabilitation
neck pain
cervical rehabilitation
neck pain
Scopo principale
Altro
Allocazione
Randomizzato
Modello di intervento
Cross-over
Mascheramento
Singolo
Bracci / Interventi
| Gruppo/Braccio di partecipanti | Intervento/Trattamento |
|---|---|
Comparatore attivoEarly cervical spine focused treatment and standard concussion care The cervical spine focused treatment will start concurrently with the standard care once the participant is randomized to this group. The participants will receive early cervical spine focused treatment 2x/week for 4 weeks. In addition to the cervical spine focused treatment, this group will also receive standard concussion care interventions individualized to the participant's needs 1x/week concurrently during the same 4-week period of time. After 4 weeks, the participant will discontinue the cervical spine focused treatment but may continue with standard concussion care for an additional 4 weeks (maximum total treatment duration is 8 weeks). | Cervical Rehabilitation * Manual joint mobilization (Grades I-V) of painful and restricted cervical spine segments.
* Supine manual cervical traction to stretch and mobilize the cervical spinal tissues.
* Manual soft tissue mobilization of the cervical, upper thoracic and/or shoulder muscles.
* Passive stretching of hypertonic muscles and active strengthening of hypotonic muscles.
* Motor-control and isometric exercises to activate the deep neck flexors. Standard Concussion Care Standard Concussion Care interventions are individualized to each patient and their adjudicated profile(s)/moderating factor(s) and may include any/all of the following:
* Behavioral regulation
* Vestibular rehabilitation
* Oculomotor rehabilitation
* Exertion rehabilitation
* Pharmacological management
* Behavioral sleep intervention
* \*Cervical spine rehabilitation (the variable of interest in this study)
* Psychotherapy |
Comparatore attivoStandard concussion care alone followed by delayed cervical spine focused treatment Participants randomized to the delayed cervical spine focused treatment group will only receive the standard concussion care (individualized to their needs) 1x/week for the initial 4 weeks. At the 4-week timepoint, the cervical spine focused treatment will be added to the standard concussion care at a frequency of twice a week for 4 weeks. Should a participant be cleared for return to activity prior to the end of the 4-week period, cervical spine focused treatment will be suspended. The maximum total treatment duration is 8 weeks; 1x/week for weeks 1-8 for the standard concussion care and 2x/week for weeks 4-8 for the cervical spine focused treatment. | Cervical Rehabilitation * Manual joint mobilization (Grades I-V) of painful and restricted cervical spine segments.
* Supine manual cervical traction to stretch and mobilize the cervical spinal tissues.
* Manual soft tissue mobilization of the cervical, upper thoracic and/or shoulder muscles.
* Passive stretching of hypertonic muscles and active strengthening of hypotonic muscles.
* Motor-control and isometric exercises to activate the deep neck flexors. Standard Concussion Care Standard Concussion Care interventions are individualized to each patient and their adjudicated profile(s)/moderating factor(s) and may include any/all of the following:
* Behavioral regulation
* Vestibular rehabilitation
* Oculomotor rehabilitation
* Exertion rehabilitation
* Pharmacological management
* Behavioral sleep intervention
* \*Cervical spine rehabilitation (the variable of interest in this study)
* Psychotherapy |
Esito primario
Esito secondario
| Misure di esito | Descrizione della misura | Arco temporale |
|---|---|---|
Recruitment rate | Enrolling 6 new participants per month | 6 months |
Treatment Adherence | Assess the rate of adherence to treatment with a goal of participant attending ≥ 75% (6 of 8) of scheduled visits. | 2 months |
Conversion Rate | Ratio of concussion patients with neck pain approached about participation or referred for screening to those actually screened. As well as conversion rate of concussion patients screened for participation to those enrolled and randomized. | 6 months |
Adverse Event Rate | Rates of expected side effects and adverse events | 2 months |
| Misure di esito | Descrizione della misura | Arco temporale |
|---|---|---|
Concussion Clinical Profile screen (CP screen) | Patient reported outcome regarding their concussion symptoms. The raw score ranges from 0 to 87. The scale helps identify specific clinical profiles and associated modifiers in concussion patients. | Baseline, 4 week, 8 week |
Numeric pain rating scale (NPRS) | Patient reported measure regarding average neck pain over past week. The score range from 0 to 10 where 0 is no pain and 10 is considered the worst pain imaginable. | Baseline, 4 week, 8 week |
Neck Disability index (NDI) | Patient reported outcome regarding their neck pain related disability. The scale ranges from 0-50 that are then converted to percentages. The scores are interpreted as: 0-20%: minimal disability; 21-40%: moderate disability; 41-60%: severe disability; and \>60%: complete disability. | Baseline, 4 week, 8 week |
Pain, Enjoyment and General Activity Score (PEG) | Patient reported outcome regarding their pain and its interference to enjoyment in life and general activity in the past week. The scale has three individual items that are scored from 0 to 10. The overall score is the average of the three individual item scores rounded to the nearest whole number for clinical use. | Baseline, 4 week, 8 week |
Criteri di eleggibilità
Età idonea
Bambino, Adulto
Età minima
12 Years
Sessi idonei
Tutti
- Diagnosed concussion
- Patient endorses neck pain OR difficulty moving their neck (moderate or severe; score of 2 or 3 for items 16 and 25 from concussion CP screen)
- Willingness to be randomized
- 8-90 days post injury
- English Speaking
- Previous concussion within the past 6 months
- Prior history of ischemic/vascular events
- Previous treatment for current symptoms
- Prior treatment for neck pain/headaches in the past year
- Workers' compensation claim and/or litigation associated with injury
- Diagnosed substance use disorder
- Prior cervical spine surgery
- Prior fracture and or dislocation/subluxation of the cervical spine
- Diagnosed inflammatory arthritis
Università di Pittsburgh543 studi clinici attivi da esplorareParte responsabile dello studio
Michael Schneider, DC, PhD, Investigatore principale, Professor, University of Pittsburgh
Contatti principali dello studio
Contatto: Cynthia L Holland, MPH, 4129046126, [email protected]
4 Centri dello studio in 3 paesi
Pennsylvania
UPMC sports medicine, Pittsburgh, Pennsylvania, 15203, United States
Cynthia L Holland, Contatto, 4129046126, [email protected]
In arruolamento
Wisconsin
Greenfield Clinic-Children's Wisconsin, Milwaukee, Wisconsin, 53227, United States
Jeff King, DC, Contatto, 2628255139, [email protected]
Amy Nader, Contatto, 4149557314, [email protected]
Non ancora in arruolamento
UPMC Sports Surgery Clinic, Dublin, Ireland
Ciaran Cosgrave, Contatto, +353 1 526 2030, [email protected]
Louise Keating, Contatto, +353 1 4022259, [email protected]
Non ancora in arruolamento
Sports Medicine Northern Ireland, Belfast, United Kingdom
Alan Rankin, Contatto, 028 9019 0290, [email protected]
Louise Keating, Contatto, +353 1 4022259, [email protected]
Non ancora in arruolamento