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Clinical Trials/NCT06015451
NCT06015451RecruitingNot Applicable

Exercise Interventions in Patients With Postconcussion Symptoms and Posttraumatic Headache. A Randomized Controlled Trial.

St. Olavs Hospital1 site in 1 country100 target enrollmentStarted: November 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
Exercise tolerance

Study Overview

Brief Summary

The goal of this clinical trial is to compare two models of delivery of guided exercise in patients with exercise intolerance after mild head injury.

The main question it aims to answer is:

• Is a program that includes elements of in-house exercise and follow-up sessions, and repeated treadmill testing, superior to a program with telephone-based follow-up only?

Participants will undergo a treadmill test to determine eligibility for the study, and to determine at what intensity level their symptoms worsen (symptom threshold). Thereafter they will exercise 15-20 minutes, 3-5 times per week at 80-90% of the heart rate that was found to be the symptom threshold. One group will receive face-to-face folllow-up and repeated testing, one group will receive telephone-based follow-up only .

Researchers will compare these two groups to see if closer follow-up is superior when it comes to recovery from exercise intolerance after 12 weeks of exercise.

Detailed Description

Patients with self-reported symptom exacerbation in relation to physical activity will be screened for inclusion with Buffalo Concussion Treadmill test (BCTT), an incremental treadmill exercise test according to a standard Balke protocol, to the first sign of symptom exacerbation or submaximal exertion. Heart rate and perceived exertion (Borg scale) are measured every minute. Patients who demonstrate symptom exacerbation according to predefined criteria will receive an individually tailored program for workouts with self-selected aerobic activites, of 15-20 minutes duration, 4-5 times per week at 85-90% (measured with HR monitor) of the HR at test termination, and they are randomised to either:

A. Every week the first three weeks, participants will exercise one individual session at the hospital, and the BCTT will be performed every 3rd week at the hospital to be able to shape the intervention.

B. The participants will only exercise at home, and will be contacted by telephone/video call, every week during the first three weeks, thereafter less often, up to every third week.

After 12 weeks, there will be a repeated BCTT, performed by a blinded assessor.

Patient reported outcomes are collected using electronic questionnaires before and after the intervention and 6 months after inclusion.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Masking Description

The treadmill test after completion of intervention is performed by an assessor that is blinded for group membership.

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age 18-65 years
  • •Having sustained a minimal head injury or mild traumatic brain injury at least 2 weeks ago.
  • •At least one postconcussion symptoms, of at least moderate degree, occurring within the first week after the head injury.
  • •Intolerance for physical activity (self-reported and measured; including symptom exacerbation later on the test day).
  • •Capable of giving informed consent.

Exclusion Criteria

  • •More than 2 years since last injury.
  • •The symptoms are better explained by other conditions.
  • •Severe communication problems, typically due to poor knowledge of Norwegian.
  • •Severe psychiatric, neurological, somatic, or substance abuse disorders that will make it problematic to function in a group and/or will complicate follow-up and outcome assessment.
  • •Safety concerns according to the study medical checklist.

Arms & Interventions

Follow-up face-to face

Active Comparator

Home-based and in-house exercise, supervised both by telephone and face-to-face.

Every week the first three weeks participants will exercise one session at the hospital, and the BCTT/BCCT will be performed every 3rd week, at the hospital in order to be able to shape the intervention.

Intervention: Sub-symptom threshold exercise (Other)

Follow-up over the phone

Active Comparator

Home-based exercise only, supervised by telephone. The participants will exercise solely in the home setting and will be contacted by telephone, every week during the first three weeks, thereafter every third week. Based on the therapist's evaluation during these calls, the intervention is shaped.

Intervention: Sub-symptom threshold exercise (Other)

Outcomes

Primary Outcomes

Exercise tolerance

Time Frame: 3 months

Change in heart rate at test termination (the Buffalo Concussion Treadmill Test)

Secondary Outcomes

  • Headache burden(6 months)
  • Depressive symptoms(6 months)
  • Change on self-selected area of function.(6 months)
  • Self-reported amount of physical activity(6 months)
  • Anxiety(6 months)
  • Impact of headaches(6 months)
  • Quality of life after head injury (QOL)(6 months)
  • Fatigue(6 months)
  • Adherence to training(6 months)

Investigators

Sponsor
St. Olavs Hospital
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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