Ignite Creation Date:
2025-12-24 @ 12:18 PM
Ignite Modification Date:
2025-12-27 @ 9:33 PM
Study NCT ID:
NCT04878861
Status:
UNKNOWN
Last Update Posted:
2021-05-10
First Post:
2021-04-28
Is Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Rehabilitating Visual Deficits Caused by Stroke
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D006423', 'term': 'Hemianopsia'}, {'id': 'D020521', 'term': 'Stroke'}], 'ancestors': [{'id': 'D014786', 'term': 'Vision Disorders'}, {'id': 'D012678', 'term': 'Sensation Disorders'}, {'id': 'D009461', 'term': 'Neurologic Manifestations'}, {'id': 'D009422', 'term': 'Nervous System Diseases'}, {'id': 'D001766', 'term': 'Blindness'}, {'id': 'D005128', 'term': 'Eye Diseases'}, {'id': 'D012816', 'term': 'Signs and Symptoms'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}, {'id': 'D002561', 'term': 'Cerebrovascular Disorders'}, {'id': 'D001927', 'term': 'Brain Diseases'}, {'id': 'D002493', 'term': 'Central Nervous System Diseases'}, {'id': 'D014652', 'term': 'Vascular Diseases'}, {'id': 'D002318', 'term': 'Cardiovascular Diseases'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 20}}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'RECRUITING', 'startDateStruct': {'date': '2020-12-13', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2021-05', 'completionDateStruct': {'date': '2024-10-16', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2021-05-06', 'studyFirstSubmitDate': '2021-04-28', 'studyFirstSubmitQcDate': '2021-05-06', 'lastUpdatePostDateStruct': {'date': '2021-05-10', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2021-05-10', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2024-10-16', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Change in motion discrimination thresholds after 6 months of training', 'timeFrame': '6 months', 'description': 'Change in normalised discrimination thresholds on psychophysical motion discrimination task at two trained locations between baseline (0-month) and 6-month follow up. These assessments will be based on what motion can be reliably detected at a 75% correct level of performance.'}], 'secondaryOutcomes': [{'measure': 'Maintenance of improvement in motion discrimination thresholds at 9-month follow up.', 'timeFrame': '9 months', 'description': 'No change in normalised discrimination thresholds on psychophysical motion discrimination task at two trained locations between 6-month and 9-month follow up. These assessments will be based on what motion can be reliably detected at a 75% correct level of performance.'}, {'measure': 'Change in area improved on the Humphrey perimetry (24-2 and 10-2)', 'timeFrame': '6 months', 'description': 'Change in area improved on a composite measure of deficit size calculated from 24-2 and 10-2 across both eyes. Area of improvement will be calculated as the area where the sensitivity improved by more than 6 decibels (dB) relative to pre-training.'}, {'measure': 'Maintenance area improved on the Humphrey perimetry (24-2 and 10-2)', 'timeFrame': '9 months', 'description': 'No change in area improved on a composite measure of deficit size calculated from 24-2 and 10-2 across both eyes. Area of improvement will be calculated as the area where the sensitivity improved by more than 6dB relative to pre-training.'}, {'measure': 'Change in contrast detection at trained locations', 'timeFrame': '6 months', 'description': 'Change in detection of stimulus at 1%, 5%, 10%, 50% and 100% contrast baseline (0-month) and 6-month follow up.'}, {'measure': 'Maintenance contrast detection at trained locations', 'timeFrame': '9 months', 'description': 'No change in detection of stimulus at 1%, 5%, 10%, 50% and 100% contrast between the 6-month and 9-month follow up.'}, {'measure': 'Change in visual quality of life', 'timeFrame': '6 months', 'description': 'Change on the Visual Function Questionnaire 25 between baseline (0-month) and 6-month follow up.'}, {'measure': 'Maintenance of visual quality of life', 'timeFrame': '9 months', 'description': 'No change in visual quality of life as measured by the Visual Function Questionnaire 25 between 6-month and 9-month follow up.'}, {'measure': 'Change in white matter integrity', 'timeFrame': '6 months', 'description': 'Change in white matter integrity in lateral geniculate nucleus (LGN) to extrastriate motion area (hMT+) and LGN to primary visual cortex (V1) tracts between baseline (0-month) and 6-month follow up, assessed by diffusion-weighted imaging'}, {'measure': 'Maintenance of white matter integrity', 'timeFrame': '9 months', 'description': 'No change of integrity in LGN-hMT+ and LGN-V1 tracts between 6-month and 9-month follow up, assessed by diffusion-weighted imaging.'}, {'measure': 'Change in neurochemistry', 'timeFrame': '6 months', 'description': 'Change in neurochemistry in visual motion area, hMT+ between baseline (0-month) and 6-month follow up, assessed by Magnetic Resonance Spectroscopy (MRS).'}, {'measure': 'Maintenance of neurochemistry', 'timeFrame': '9 months', 'description': 'No change in neurochemistry in visual motion area, hMT+ between 6-month and 9-month follow up, assessed by Magnetic Resonance Spectroscopy (MRS).'}, {'measure': 'Change in brain activity during visual stimulation (Blood-oxygen-level-dependent imaging, or BOLD, signal change)', 'timeFrame': '6 months', 'description': 'Change in brain activity during moving visual stimulation, assessed by functional magnetic resonance imaging (BOLD signal) in visual motion area, hMT+ between baseline (0 month) and 6-month follow up.'}, {'measure': 'Maintenance of brain activity during visual stimulation (BOLD signal change)', 'timeFrame': '9 months', 'description': 'Maintenance of brain activity during moving visual stimulation, assessed by functional magnetic resonance imaging (BOLD signal) in visual motion area, hMT+ between the 6-month and 9-month follow up.'}, {'measure': 'Change in resting state connectivity', 'timeFrame': '6 months', 'description': 'Change in resting state connectivity in the visual cortex between baseline (0-months) and 6-months, assessed by resting state functional magnetic resonance imaging (BOLD signal)'}, {'measure': 'Maintenance of resting state connectivity', 'timeFrame': '9 months', 'description': 'Maintenance of resting state connectivity in the visual cortex between 6-month and 9-month follow up, assessed by resting state functional magnetic resonance imaging (BOLD signal)'}]}, 'oversightModule': {'isUsExport': True, 'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['Vision', 'Stroke', 'Visual training', 'Blindsight', 'Visual pathway'], 'conditions': ['Hemianopia', 'Hemianopsia', 'Quadrantanopia', 'Stroke Induced Vision Loss']}, 'descriptionModule': {'briefSummary': 'This research aims to understand the efficacy of a visual training task to improve visual loss after stroke, also known as hemianopia. The investigators aim to understand whether training can improve vision and which areas or pathways in the brain are responsible for this improvement.', 'detailedDescription': 'Damage to the primary visual cortex (V1) due to stroke usually results in loss of visual function in half of the visual world, this is known as hemianopia. This visual loss can negatively affect quality of life, as most stroke survivors are no longer permitted to drive and have difficulties with navigation and socialising. There are currently limited treatment options, although recent evidence suggests that visual training can be effective in improving visual function (Huxlin et al, 2009; Cavanaugh \\& Huxlin, 2017). The aim of this research is to determine the capacity for visual rehabilitation after stroke using visual training and to understand the underlying brain mechanisms that might drive these improvements. This study will help the investigators to understand the brain mechanisms involved in visual rehabilitation and may allow the investigators to predict those most likely to benefit from visual rehabilitation in the future.\n\nTwenty stroke survivors with hemi- or quadrantanopia will complete a 6-month visual motion discrimination training programme at home. Each participant will have three study visits; at baseline, 6-months and 9-months. At each visit the investigators will take measures of 1) visual fields 2) detailed tests of visual function 3) quality of life and 4) MRI scans of brain structure, function and neurochemistry. Between the baseline (0 month) and 6-month post-training session, participants will complete visual training at home. Between the 6-month post-training session and 9-month follow up, participants will not complete visual training at home. This study will therefore allow the investigators to determine whether rehabilitation improves conscious visual perception and quality of life as well as providing understanding of the neural mechanisms that underlie this improvement. The investigators will also determine whether improvements or neural changes persist after 3-months without training.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '80 Years', 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Aged 18-80\n* Participant is willing and able to give informed consent for participation in the study\n* Fluent English-speaking healthy adults\n* Has suffered damage to the visual cortex at least 6 months before the study\n\nExclusion Criteria:\n\n* Previous eye disease or impairment other than hemianopia\n* Neurological or psychiatric illness\n* Contraindication to MRI\n* Pregnant or breast feeding\n* Second stroke during training\n\nData quality assurance (participant data will be removed from analysis for the following reasons):\n\n* Concurrent participation in other "vision therapy"\n* Unreliable visual fields, indicated by greater than 20% fixation losses, false positives, or false negatives\n* Inability to demonstrate fixation stability on eye movement monitored testing\n* Failure to complete at least 100 training sessions over 6-months'}, 'identificationModule': {'nctId': 'NCT04878861', 'briefTitle': 'Rehabilitating Visual Deficits Caused by Stroke', 'organization': {'class': 'OTHER', 'fullName': 'University of Oxford'}, 'officialTitle': 'Rehabilitating Visual Deficits Caused by Stroke: Neurochemical and Neurophysiological Markers for Optimal Recovery', 'orgStudyIdInfo': {'id': 'R60132/RE001'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Training in blind field', 'description': 'All participants undergo this intervention. Internal control is comparing sighted and non-sighted parts of the field.', 'interventionNames': ['Behavioral: Training in the blind field']}], 'interventions': [{'name': 'Training in the blind field', 'type': 'BEHAVIORAL', 'description': 'Participants will complete visual training at two locations in the blind field. These two locations of training will be determined at the baseline study visit (0 months) and will be located within the perimetry-defined blind field. The training programme involves discriminating the direction of motion in a small circle of moving dots. The computer software and a chin-rest will be loaned to each participant to complete training at home. Participants will perform 300 trials at each location in their blind field, 5 days a week for at least 24 weeks (40-60 minutes in total). The computer programme will automatically generate a record of participant performance after each home training session.', 'armGroupLabels': ['Training in blind field']}]}, 'contactsLocationsModule': {'locations': [{'zip': 'OX3 9DU', 'city': 'Oxford', 'state': 'Oxfordshire', 'status': 'RECRUITING', 'country': 'United Kingdom', 'contacts': [{'name': 'Hannah Willis, MPsych', 'role': 'CONTACT', 'email': 'hannah.willis@ndcn.ox.ac.uk', 'phone': '01865 611458'}, {'name': 'Holly Bridge, DPhil', 'role': 'CONTACT', 'email': 'holly.bridge@ndcn.ox.ac.uk', 'phone': '01865 610482'}, {'name': 'Holly Bridge, DPhil', 'role': 'PRINCIPAL_INVESTIGATOR'}, {'name': 'Hannah Willis, MPsych', 'role': 'SUB_INVESTIGATOR'}, {'name': 'Kate Watkins, PhD', 'role': 'SUB_INVESTIGATOR'}, {'name': 'Krystel Huxlin, PhD', 'role': 'SUB_INVESTIGATOR'}, {'name': 'Marco Tamietto, PhD', 'role': 'SUB_INVESTIGATOR'}, {'name': 'Matthew Cavanaugh, PhD', 'role': 'SUB_INVESTIGATOR'}], 'facility': 'Wellcome Centre For Integrative Neuroimaging, University of Oxford', 'geoPoint': {'lat': 51.75222, 'lon': -1.25596}}], 'centralContacts': [{'name': 'Hannah Willis, MPsych', 'role': 'CONTACT', 'email': 'hannah.willis@ndcn.ox.ac.uk', 'phone': '01865 611458'}, {'name': 'Holly Bridge, PhD', 'role': 'CONTACT', 'email': 'holly.bridge@ndcn.ox.ac.uk', 'phone': '01865 610482'}], 'overallOfficials': [{'name': 'Holly Bridge, PhD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'University of Oxford'}]}, 'ipdSharingStatementModule': {'timeFrame': 'After conclusion of study.', 'ipdSharing': 'YES', 'description': 'We plan to share subsets of the data as appropriate.'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'University of Oxford', 'class': 'OTHER'}, 'collaborators': [{'name': 'University of Rochester', 'class': 'OTHER'}, {'name': 'University of Turin, Italy', 'class': 'OTHER'}, {'name': 'University of Texas at Austin', 'class': 'OTHER'}], 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'Professor', 'investigatorFullName': 'DrHollyBridge', 'investigatorAffiliation': 'University of Oxford'}}}}