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Effectiveness of Early Physical Therapy Intervention for Patients With Dizziness After a Sports-Related Concussion

Primary Purpose

Brain Concussion, Dizziness

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Physical Therapy Treatment
Sponsored by
Walsh University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Concussion

Eligibility Criteria

10 Years - 23 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients age 10 - 23 who have sustained a sports-related concussion.
  • Sports will include participation in any organized sporting activity (including club teams, recreational sports, or school teams).
  • Patients with a history of learning disorders, use of medication (including psychotropics or narcotics) will be included.

Exclusion Criteria:

  • Patients younger than 10 years or older than 23 years of age.
  • If the patient has a concussion that was sustained during activities other than sports-related (bicycle accident, motor vehicle accident, or other non-sports related activities) they will not be enrolled in this study.
  • Athletes with concussion who have symptoms but none of their complaints include dizziness or indicate a postural/vestibular/ocular or perceptual abnormality will be excluded.
  • Finally, athletes who present to the sports-medicine physician for an initial assessment greater than 14 days after they sustained a concussion will be excluded.

Sites / Locations

  • Walsh University

Arms of the Study

Arm 1

Arm 2

Arm Type

Sham Comparator

Experimental

Arm Label

Minimally Therapeutic Treatment

Skilled Treatment

Arm Description

Non-differential, prescriptive protocol of physical therapy treatment with minimal to no therapeutic benefit.

Differential treatment based on the results from the assessment. Physical Therapy treatment in this arm will be pragmatically designed and modified by the treating therapist. Treatments will include manual therapy to the cervical spine, neuromotor retraining (position sense and movement sense), habituation and adaptation exercises.

Outcomes

Primary Outcome Measures

Symptom recovery as measured by the Post Concussion Symptom (PCS) Score
7 point Likert scale (0 - 6) rating the severity of 22 symptoms commonly associated with concussion.
Return to Play (RTP)
Five stage progressive increase in physical activity ranging from minimal exertion to full contact in a game

Secondary Outcome Measures

Change Score of Functional Gait Assessment
Used to test balance with gait activities.
Change score of Vertigo Symptom Scale - Short Form
Frequency of various types and durations of sensation of dizziness
Global Response to Treatment
Global perception of change in physical symptoms from the beginning of treatment to the end

Full Information

First Posted
November 17, 2014
Last Updated
February 24, 2016
Sponsor
Walsh University
Collaborators
Children's Hospital Medical Center of Akron, Kent State University, American Academy of Orthopaedic Manual Physical Therapists, Ohio Physical Therapy Association
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1. Study Identification

Unique Protocol Identification Number
NCT02299128
Brief Title
Effectiveness of Early Physical Therapy Intervention for Patients With Dizziness After a Sports-Related Concussion
Official Title
A Feasibility Study for a Randomized Controlled Trial on the Effectiveness of Early Physical Therapy Intervention for Patients With Dizziness After a Sports-Related Concussion
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Completed
Study Start Date
September 2014 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
January 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Walsh University
Collaborators
Children's Hospital Medical Center of Akron, Kent State University, American Academy of Orthopaedic Manual Physical Therapists, Ohio Physical Therapy Association

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Therefore, the purpose of this pilot study is to determine the feasibility of conducting a randomized clinical trial (RCT) on physical therapist treatment for dizziness after sports-related concussion. The specific research question for this pilot RCT is: What is the feasibility of conducting a RCT on athletes who have dizziness 10 or greater days after a sports-related concussion to explore the effectiveness of directed vestibular rehabilitation, neuromotor retraining, and/or manual physical therapy (PT) when compared to sham treatment? The findings of this study (for both feasibility and effect size) will be used to inform and direct revisions to the methods for a larger RCT on this population. Primary Aims: Specific Aim 1: Assess the feasibility of the following: recruitment and retention of participants, required resources for project management, and assessment of patient safety. Specific Aim 2: Estimate the size of the effect between skilled physical therapist intervention and a sham treatment for the recovery rate for athletes with a concussion who have dizziness 10 - 14 days post-concussion.
Detailed Description
Study design: This study will be a pilot feasibility study of a RCT, randomized at the individual level. Subjects: The population of interest includes athletes who are seen by the physicians from a Sports Medicine Center (on site at Akron Children's Hospital (ACH) or at proxy locations, e.g. Walsh University or North Canton Children's Hospital Clinic) with a sports-related concussion. The specific population of interest is concussed patients who present for a medical assessment with dizziness as measured by the Post-Concussion Symptom Scale (PCS). Sample Size and Sampling: Because this is a pilot study exploring the feasibility of the recruitment, retention and methods for a larger RCT, the sample is not intended to power a full scale study. It is standard for a pilot study to include at least 12 participants per arm of the study, however, because of the potential for loss to follow up the investigators plan to enroll 20 subjects per treatment group. Study Subject Selection and Definitions: All patients who present to a Sports Medicine Center after an acute concussion (defined as any time between the event causing the concussion and up to 14 days after concussion) will complete the PCS. Within this 22 item scale, 7 items specify physical symptoms as components of the migraine cluster. These symptoms include: headaches, visual problems, dizziness, noise-light sensitivity, nausea/vomiting, balance problems, numbness/tingling. Although dizziness is the primary patient complaint being targeted, these other symptoms within the migraine cluster may also be present in addition to dizziness and may implicate a cervical, proprioceptive, and/or vestibular injury. For this reason, patients who report symptoms in the migraine cluster with one of the following criteria will be asked to enroll in the study at the initial assessment: An initial score of at least 3 on the 7 point Likert scale for dizziness as a singular symptom OR A score of 10 across the 7 items within the migraine cluster including a complaint of dizziness with at a score of at least 1 on the 7 point Likert scale OR If findings from the objective assessment conducted by the physician indicate that postural/vestibular/ocular perception is abnormal. Methods Allocation: At day10 after concussion, patients who enrolled in the study at their initial medical visit will be contacted by e-mail through Qualtrics and will be asked to complete the PCS a second time (if the patient sees the medical provider from Sports Medicine between day 10 and day 14, this will done on that same day). If at day 10 - 14 after the concussion was sustained, the patient continues to report dizziness with a score of at least 3 or a total score in the migraine cluster of at least 10 (including a score of at least 1 for dizziness) he/she will be randomized into one of the treatment groups using a random allocation sequence generator. If the patient does not meet the threshold of symptoms at day 10 - 14, they will receive standard medical care from the Sports Medicine physicians but will not be randomized into one of the PT treatment arms. One study investigator will be responsible for assignment into the treatment groups using a 1:1 allocation ratio. Blinding: This study will be conducted as a double-blind trial whereby the physicians in the sports-medicine center, the patient participants, and their families will be blinded to the treatment allocation (sham or skilled) of patients throughout the study time. Blinding here is important to limit study bias because the physicians will determine one key outcome, the timeframe for return to play, and the athletes will report on the second key outcome, symptom severity on the PCS. The PTs performing the assessment and treatments will not be blinded to the allocation of the patients as they will be delivering the intervention. The same therapists will deliver both treatments (sham and skilled) based on allocation. Because the PTs cannot be blinded to the allocation of treatment, they will not determine the timeframe for return to play. Patient follow-up: All patients allocated into one of the treatment arms will be followed for 4 consecutive weeks or until they are released for return to play by the sports medicine physician. All patients will continue to be followed by physicians in the sports medicine practice (as that is the standard of care). Patient safety: Because this study is challenging the rest paradigm and using a progressive and active treatment to manage acute dizziness, it is not without risk. Patients will be carefully monitored during each visit to determine their response to treatment. Since the sham treatment incorporates no actual therapeutic activities, an exacerbation in symptoms is not expected. The skilled treatment group is pragmatic, allowing the treating therapists to determine the type and aggressiveness of each treatment session. This gives therapists the ability to modify the activity using their expert clinical judgment. For all subjects in the study, patient response between PT sessions will be monitored at the beginning of each PT treatment. If patient symptoms increase between therapy sessions, greater than the standard error of measure 6.3 points, treatment will be ceased and patients will be referred back to Sports Medicine for follow up. All adverse events will be recorded.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Concussion, Dizziness

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
41 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Minimally Therapeutic Treatment
Arm Type
Sham Comparator
Arm Description
Non-differential, prescriptive protocol of physical therapy treatment with minimal to no therapeutic benefit.
Arm Title
Skilled Treatment
Arm Type
Experimental
Arm Description
Differential treatment based on the results from the assessment. Physical Therapy treatment in this arm will be pragmatically designed and modified by the treating therapist. Treatments will include manual therapy to the cervical spine, neuromotor retraining (position sense and movement sense), habituation and adaptation exercises.
Intervention Type
Other
Intervention Name(s)
Physical Therapy Treatment
Other Intervention Name(s)
Vestibular rehabilitation, Manual Therapy, Neuromotor training
Primary Outcome Measure Information:
Title
Symptom recovery as measured by the Post Concussion Symptom (PCS) Score
Description
7 point Likert scale (0 - 6) rating the severity of 22 symptoms commonly associated with concussion.
Time Frame
Final visit (by the end of 4 weeks of treatment)
Title
Return to Play (RTP)
Description
Five stage progressive increase in physical activity ranging from minimal exertion to full contact in a game
Time Frame
Final visit (by the end of 4 weeks of treatment)
Secondary Outcome Measure Information:
Title
Change Score of Functional Gait Assessment
Description
Used to test balance with gait activities.
Time Frame
Initial assessment and final visit (by the end of 4 weeks of treatment)
Title
Change score of Vertigo Symptom Scale - Short Form
Description
Frequency of various types and durations of sensation of dizziness
Time Frame
Initial assessment and final visit (by the end of 4 weeks of treatment)
Title
Global Response to Treatment
Description
Global perception of change in physical symptoms from the beginning of treatment to the end
Time Frame
Final Visit (by the end of 4 weeks of treatment)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
23 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients age 10 - 23 who have sustained a sports-related concussion. Sports will include participation in any organized sporting activity (including club teams, recreational sports, or school teams). Patients with a history of learning disorders, use of medication (including psychotropics or narcotics) will be included. Exclusion Criteria: Patients younger than 10 years or older than 23 years of age. If the patient has a concussion that was sustained during activities other than sports-related (bicycle accident, motor vehicle accident, or other non-sports related activities) they will not be enrolled in this study. Athletes with concussion who have symptoms but none of their complaints include dizziness or indicate a postural/vestibular/ocular or perceptual abnormality will be excluded. Finally, athletes who present to the sports-medicine physician for an initial assessment greater than 14 days after they sustained a concussion will be excluded.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer C Reneker, MSPT
Organizational Affiliation
Walsh University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Walsh University
City
North Canton
State/Province
Ohio
ZIP/Postal Code
44720
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Effectiveness of Early Physical Therapy Intervention for Patients With Dizziness After a Sports-Related Concussion

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