Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT06015451 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Exercise in Postconcussion Symptoms and Posttraumatic Headache

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 1 year 6 months later Mar 1, 2026 → Sep 1, 2027
See other at-risk trials from St. Olavs Hospital

Record History

  1. Notable Primary completion pushed from Mar 1, 2026 to Sep 1, 2027
    • Study completion pushed from Sep 1, 2026 to Sep 1, 2028
    v3
  2. Notable Primary completion date: Mar 1, 2025 to Mar 1, 2026
    • Study completion date: Sep 1, 2025 to Sep 1, 2026
    v2
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT06015451
Lead Sponsor St. Olavs Hospital
Conditions
(from sponsor)
Brain Concussion, Post-Concussion Syndrome, Post-Traumatic Headache, Craniocerebral Trauma
Related terms Brain Concussion, Craniocerebral Trauma, Motor Activity, Post-Concussion Syndrome, Post-Traumatic Headache
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov