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Feasibility of Aerobic Exercise for Recovery From Work-related Concussion

Feasibility of Aerobic Exercise for Recovery From Work-related Concussion

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06263179
Enrollment
11
Registered
2024-02-16
Start date
2024-07-01
Completion date
2025-04-30
Last updated
2025-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Concussion, Brain

Brief summary

There is a lot of research on how to treat people with sport-related concussion. There has not been a lot of research on the treatment of injured workers with concussion. An exercise program has been developed for people with sport-related concussion. It is suspected that this program may be helpful for injured workers with concussion too. This study will test the effect of this exercise in injured workers with concussion.

Detailed description

Participants who are diagnosed with a concussion and agree to participant in the study will complete a demographics form and other relevant questionnaires. They will then perform a graded exertion test (the Buffalo Concussion Treadmill Test \[BCTT\]) at the clinic, this takes approximately 15 minutes. Participants will then be prescribed the individualized THRAE based on the results from the BCTT and will be sent home with a commercial heart rate monitor. Participants will perform exercises at home on their free time 4-5 days per week. Participants will return to the clinic weekly to be re-examined by the study physician and obtain a new heart rate prescription for the first six weeks until clinical recovery or the intervention period ends (6-weeks).

Interventions

BEHAVIORALTarget Heartrate Aerobic Exercise

Exercise program

Sponsors

National Center for Advancing Translational Sciences (NCATS)
CollaboratorNIH
State University of New York at Buffalo
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Target Heartrate Aerobic Exercise

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Aged 18-40 * Received a concussion at work and are engaged with the workers compensation program * Within 3 weeks of concussive injury

Exclusion criteria

* 3-point or less difference between current and pre-injury symptoms as measured by the Post-Concussion Symptom Inventory (PCSI) * Moderate or severe TBI * Injury involving loss of consciousness for \>30 minutes or post-traumatic amnesia \> 24 hours * Pre-existing conditions or presence of polytrauma that prevent participation in active testing and/or rehabilitation * History of more than 3 diagnosed concussions * Active substance abuse/dependence * Report of injury mechanism occurring due to physical assault * Unwillingness to perform intervention * Limited English proficiency.

Design outcomes

Primary

MeasureTime frameDescription
Adherence to Target Heartrate Aerobic Exercise (THRAE) program as measured by counting the number and duration of exercise sessions completed.Up to 6 weeksAdherence to Target Heartrate Aerobic Exercise (THRAE) program as measured by counting exercise sessions completed.

Secondary

MeasureTime frameDescription
Change in post-concussive symptom burden as measured by the Post-Concussion Symptom ScaleBaseline, week 1, week 2, week 3, week 4, week 5, week 6The Post-Concussion Symptom Scale (PCSS) is a validated 22-item self-report symptom questionnaire. Scores range from 0-132 with greater scores indicating increased symptom burden.
Change in Patient Health Questionnaire-9 (PHQ-9)Baseline, up to week 6The Patient Health Questionnaire-9 (PHQ-9) is used for rating the severity of depression among participants. Scores range from 0-27. Higher scores indicate increased severity of depression.
Change in Generalized Anxiety Disorder-7 (GAD-7)Baseline, up to week 6The Generalized Anxiety Disorder-7 (GAD-7) is used to measure the severity of anxiety among participants. Scores range from 0-21. Higher scores indicate increased severity of anxiety.
Primary Care Post Traumatic Stress Disorder (PTSD) Screen for DSM-5 (PC-PTSD-5)BaselineThe Primary Care Post Traumatic Stress Disorder (PTSD) Screen for DSM-5 (PC-PTSD-5) is used to measure probable PTSD among participants. Scores range from 0-5. Higher scores indicate increased probability of PTSD.
Work Climate Questionnaire - 6-Item VersionBaselineThe Work Climate Questionnaire - 6-Item Version is used for assessing participants' perceptions regarding the degree of autonomy supportiveness of their work managers or employers. Scores range of 6-42. Higher scores indicate a greater degree of perceived autonomy supportiveness.
Change in Basic Psychological Needs Satisfaction and Frustration Scale (BPNSFS)Baseline, up to week 6The Basic Psychological Needs Satisfaction and Frustration Scale (BPNSFS) is used to assess participant satisfaction or frustration with the psychological needs for autonomy, competence, and relatedness. The scale involves 6 subscales, including autonomy satisfaction, autonomy frustration, relatedness satisfaction, relatedness frustration, competence satisfaction, and competence frustration. Each subscale has scores ranging from 4-20. Higher scores indicate higher participant perceptions of the psychological need satisfaction or frustration reflected in the subscale. This measure will be used to assess change in psychological needs satisfaction and psychological needs frustration between the initial and final visits.
Time to return to work measured in daysUp to week 6Time to return to work as measured by difference between date of injury and date the participant is medically cleared to return to work
Change in Patient-Reported Outcomes Measurement Information System Global Health-10 (PROMIS-10)Baseline, up to week 6The Patient-Reported Outcomes Measurement Information System Global Health-10 (PROMIS-10) is used to measure general healthcare-related quality of life, including global physical health and global mental health. Both global physical health and global mental health have raw scores ranging from 4-20. Higher scores reflect higher participant ratings for global physical and mental health. This measure will be used to assess change in global physical and mental health between the initial and final visits.

Other

MeasureTime frameDescription
Rate of adverse Events as assessed by questioning the participantUp to week 6At each weekly follow-up meeting participants will be asked about any adverse events including injuries or other negative events.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026