Ignite Creation Date:
2025-12-24 @ 11:40 PM
Ignite Modification Date:
2026-02-20 @ 1:45 PM
Study NCT ID:
NCT06015451
Status:
RECRUITING
Last Update Posted:
2025-07-08
First Post:
2023-07-20
Is Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Exercise in Postconcussion Symptoms and Posttraumatic Headache
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D001924', 'term': 'Brain Concussion'}, {'id': 'D038223', 'term': 'Post-Concussion Syndrome'}, {'id': 'D051298', 'term': 'Post-Traumatic Headache'}, {'id': 'D006259', 'term': 'Craniocerebral Trauma'}, {'id': 'D009043', 'term': 'Motor Activity'}], 'ancestors': [{'id': 'D000070642', 'term': 'Brain Injuries, Traumatic'}, {'id': 'D001930', 'term': 'Brain Injuries'}, {'id': 'D001927', 'term': 'Brain Diseases'}, {'id': 'D002493', 'term': 'Central Nervous System Diseases'}, {'id': 'D009422', 'term': 'Nervous System Diseases'}, {'id': 'D020196', 'term': 'Trauma, Nervous System'}, {'id': 'D016489', 'term': 'Head Injuries, Closed'}, {'id': 'D014947', 'term': 'Wounds and Injuries'}, {'id': 'D014949', 'term': 'Wounds, Nonpenetrating'}, {'id': 'D051271', 'term': 'Headache Disorders, Secondary'}, {'id': 'D020773', 'term': 'Headache Disorders'}, {'id': 'D001519', 'term': 'Behavior'}]}}, 'documentSection': {'largeDocumentModule': {'largeDocs': [{'date': '2022-10-10', 'size': 569107, 'label': 'Study Protocol and Statistical Analysis Plan', 'hasIcf': False, 'hasSap': True, 'filename': 'Prot_SAP_000.pdf', 'typeAbbrev': 'Prot_SAP', 'uploadDate': '2023-07-20T04:23', 'hasProtocol': True}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['OUTCOMES_ASSESSOR'], 'maskingDescription': 'The treadmill test after completion of intervention is performed by an assessor that is blinded for group membership.'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 100}}, 'statusModule': {'overallStatus': 'RECRUITING', 'startDateStruct': {'date': '2022-11-01', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-07', 'completionDateStruct': {'date': '2026-09-01', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-07-07', 'studyFirstSubmitDate': '2023-07-20', 'studyFirstSubmitQcDate': '2023-08-24', 'lastUpdatePostDateStruct': {'date': '2025-07-08', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2023-08-29', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2026-03-01', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Exercise tolerance', 'timeFrame': '3 months', 'description': 'Change in heart rate at test termination (the Buffalo Concussion Treadmill Test)'}], 'secondaryOutcomes': [{'measure': 'Headache burden', 'timeFrame': '6 months', 'description': 'Change in days of headache of at least moderate intensity'}, {'measure': 'Change on self-selected area of function.', 'timeFrame': '6 months', 'description': 'Change on the Patient-specific Function Scale (PSFS), the first 3 items, range 0-30, highest is worst.'}, {'measure': 'Self-reported amount of physical activity', 'timeFrame': '6 months', 'description': 'Change on the International Physical Activity Questionnaire (IPAQ), higher total values indicate more physical activity.'}, {'measure': 'Quality of life after head injury (QOL)', 'timeFrame': '6 months', 'description': 'Change on the Quality of life after brain injury - Overall Scale (QOLIBRI - OS). Six items rated on an ordinal scale, higher score indicate better QOL.'}, {'measure': 'Depressive symptoms', 'timeFrame': '6 months', 'description': 'Change on the Patient Health Questionnaire (PHQ-9). Nine items range 0-3, higher score indicates more severe depressive symptoms.'}, {'measure': 'Anxiety', 'timeFrame': '6 months', 'description': 'Change on the Generalized Anxiety Disorder Scale (GAD-7). Seven items range 0-3, higher score indicates more severe symptoms of anxiety.'}, {'measure': 'Impact of headaches', 'timeFrame': '6 months', 'description': 'Change on the Headache Impact Test (HIT)-6. Six items, Total score ranges from 36-78, higher score indicates higher impact.'}, {'measure': 'Fatigue', 'timeFrame': '6 months', 'description': 'Change on the Fatigue Severity Scale (FSS). Nina items, total score range 9-63, higher score indicates more severe fatigue.'}, {'measure': 'Adherence to training', 'timeFrame': '6 months', 'description': 'The Problematic Experience of Therapy scale (PETS). 12 questions with responses on a Likert scale. No total score.'}]}, 'oversightModule': {'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['exercise intolerance', 'exercise', 'Thread mill test'], 'conditions': ['Brain Concussion', 'Post-Concussion Syndrome', 'Post-Traumatic Headache', 'Craniocerebral Trauma']}, 'descriptionModule': {'briefSummary': '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.\n\nThe main question it aims to answer is:\n\n• 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?\n\nParticipants 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 .\n\nResearchers 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.', 'detailedDescription': '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:\n\nA. 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.\n\nB. 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.\n\nAfter 12 weeks, there will be a repeated BCTT, performed by a blinded assessor.\n\nPatient reported outcomes are collected using electronic questionnaires before and after the intervention and 6 months after inclusion.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '65 Years', 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Age 18-65 years\n* Having sustained a minimal head injury or mild traumatic brain injury at least 2 weeks ago.\n* At least one postconcussion symptoms, of at least moderate degree, occurring within the first week after the head injury.\n* Intolerance for physical activity (self-reported and measured; including symptom exacerbation later on the test day).\n* Capable of giving informed consent.\n\nExclusion Criteria:\n\n* More than 2 years since last injury.\n* The symptoms are better explained by other conditions.\n* Severe communication problems, typically due to poor knowledge of Norwegian.\n* 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.\n* Safety concerns according to the study medical checklist.'}, 'identificationModule': {'nctId': 'NCT06015451', 'briefTitle': 'Exercise in Postconcussion Symptoms and Posttraumatic Headache', 'organization': {'class': 'OTHER', 'fullName': 'St. Olavs Hospital'}, 'officialTitle': 'Exercise Interventions in Patients With Postconcussion Symptoms and Posttraumatic Headache. A Randomized Controlled Trial.', 'orgStudyIdInfo': {'id': '468196'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'ACTIVE_COMPARATOR', 'label': 'Follow-up face-to face', 'description': 'Home-based and in-house exercise, supervised both by telephone and face-to-face.\n\nEvery 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.', 'interventionNames': ['Other: Sub-symptom threshold exercise']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Follow-up over the phone', 'description': "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.", 'interventionNames': ['Other: Sub-symptom threshold exercise']}], 'interventions': [{'name': 'Sub-symptom threshold exercise', 'type': 'OTHER', 'description': 'Aerob exercise at an intensity just below the intensity that provokes symptom exacerbation.', 'armGroupLabels': ['Follow-up face-to face', 'Follow-up over the phone']}]}, 'contactsLocationsModule': {'locations': [{'zip': '7050', 'city': 'Trondheim', 'status': 'RECRUITING', 'country': 'Norway', 'contacts': [{'name': 'Toril Skandsen, PhD', 'role': 'CONTACT', 'email': 'toril.skandsen@ntnu.no', 'phone': '+47 92692780'}, {'name': 'Janne-Birgitte BB Børke, Msc', 'role': 'CONTACT', 'email': 'janne.borke@stolav.no'}], 'facility': 'St. Olavs Hospital, Clinic of Rehabilitation', 'geoPoint': {'lat': 63.43049, 'lon': 10.39506}}], 'centralContacts': [{'name': 'Toril Skandsen, PhD', 'role': 'CONTACT', 'email': 'toril.skandsen@ntnu.no', 'phone': '+4792692780'}, {'name': 'Janne-Birgitte BB Børke, MSc', 'role': 'CONTACT', 'email': 'janne.borke@stolav.no'}], 'overallOfficials': [{'name': 'Britt-Elin Lurud, MD', 'role': 'STUDY_DIRECTOR', 'affiliation': 'Clinic of Rehabilitation, St. Olavs Hospital'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'St. Olavs Hospital', 'class': 'OTHER'}, 'responsibleParty': {'type': 'SPONSOR'}}}}