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- Klinische Studie NCT07606300
Effect of Fixation Training With Colored Light Targets on Traumatic Brain Injury-Associated Photophobia
Studienübersicht
Status
Intervention / Behandlung
Detaillierte Beschreibung
A growing number of clinicians are regularly using fixation training, in which patients undergo daily sessions fixating on colored light targets on light boxes, to treat symptoms including photophobia associated with traumatic brain injury (TBI). While fixation training using various colored light targets is reported, blue light targets specifically appear to be used in this patient population more often than other light target colors. The College of Syntonic Optometry (www.csovision.org) estimates that there are roughly 500 practicing optometrists that utilize fixation training in the USA alone. However, evidence supporting this approach is primarily anecdotal, and there are no controlled, masked clinical trials published that evaluate the efficacy of this therapy against a control group.
Therefore, the goal of this study is to assess whether daily 20 min fixation training sessions using a blue light target alleviates symptoms of light sensitivity and alters pupil response more than daily 20 min fixation training sessions using red light targets in a masked cross-over clinical trial involving participants with chronic TBI-associated photophobia. In addition, we will determine if any improvement in symptomology correlates to any changes in pupil responses to red, blue and white light pulses and potential changes in other standard clinical measures of visual function. In short, this study will compare the effect of fixation training using a blue light target to the effect of fixation training using a red light target in participants with chronic TBI-associated photophobia.
Studientyp
Einschreibung (Geschätzt)
Phase
- Unzutreffend
Kontakte und Standorte
Studienkontakt
- Name: Andrew Hartwick, OD, PhD
- Telefonnummer: 16146888308
- E-Mail: HARTWICK.4@osu.edu
Studienorte
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Ohio
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Columbus, Ohio, Vereinigte Staaten, 43210
- Rekrutierung
- College of Optometry
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Kontakt:
- Andrew Hartwick, OD, PhD
- Telefonnummer: 614-688-8308
- E-Mail: HARTWICK.4@osu.edu
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- 18 to 80 years old and subjects able to consent for themselves
- Completion of first session in entirety (participants who cannot complete the entire first visit will be considered as a screen fail)
- Best-corrected visual acuity of at least 20/32 in both the right and left eyes, and 20/25 using both eyes
- Prior head injury with current photophobia - A mild or moderate TBI occurring at least 3 months prior to visit, verified by a score of 2, 3 or 4 on OSU-TBI survey, and participant reports having experienced greater light sensitivity since their head injury
Exclusion Criteria:
- Pregnancy or suspected pregnancy - based on self-report
- Previous history of neurodegenerative disease (e.g. Alzheimer's, Parkinson's, multiple sclerosis, myasthenia gravis, seizures)
- History of pathology of the retina and optic nerve (includes retinal tears, diabetic retinopathy, glaucoma, macular degeneration, optic nerve atrophy)
- Currently on cholinergic medications, which affect pupil responses
- Prior participation in fixation training sessions within the past 2 years
- Experiencing a migraine during visit
- Prior history of severe TBI (score of 5 or 6 on OSU-TBI survey)
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Crossover-Aufgabe
- Maskierung: Doppelt
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: Red light first, blue light second
Red light first, blue light second for the colored target used in the fixation training
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Red versus blue targets in light boxes used for fixation training
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Experimental: Blue light first, red light second
Blue light first, red light second for the colored target used in the fixation training
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Red versus blue targets in light boxes used for fixation training
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Pupil Responses
Zeitfenster: From baseline visit to the end of 3 months of fixation training with each light color
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Pupil responses to red, blue and white light stimuli
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From baseline visit to the end of 3 months of fixation training with each light color
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Symptom Survey
Zeitfenster: From baseline visit to the end of 3 months of fixation training with each light color
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Symptom survey
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From baseline visit to the end of 3 months of fixation training with each light color
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Vergence facility
Zeitfenster: From baseline visit to the end of 3 months of fixation training with each light color
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Measurement of vergence range (how well eyes work together) with loose prisms
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From baseline visit to the end of 3 months of fixation training with each light color
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Stereopsis
Zeitfenster: From baseline visit to the end of 3 months of fixation training with each light color
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Measurement of local stereopsis (depth perception) with Randot test
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From baseline visit to the end of 3 months of fixation training with each light color
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Phoria magnitude
Zeitfenster: From baseline visit to the end of 3 months of fixation training with each light color
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Measure of phorias (how well eyes are aligned) using cover test and loose prisms
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From baseline visit to the end of 3 months of fixation training with each light color
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Near Point of Convergence
Zeitfenster: From baseline visit to the end of 3 months of fixation training with each light color
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Measure of ability for eyes to converge (how well eyes turn in when reading up close)
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From baseline visit to the end of 3 months of fixation training with each light color
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Mitarbeiter und Ermittler
Sponsor
Mitarbeiter
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Neurologische Manifestationen
- Erkrankungen des Gehirns
- Erkrankungen des zentralen Nervensystems
- Erkrankungen des Nervensystems
- Wunden und Verletzungen
- Augenkrankheiten
- Sehstörungen
- Empfindungsstörungen
- Kraniozerebrales Trauma
- Trauma, Nervensystem
- Kopfverletzungen, geschlossen
- Wunden, nicht durchdringend
- Hirnverletzungen
- Pathologische Zustände, Anzeichen und Symptome
- Anzeichen und Symptome
- Hirnverletzungen, traumatisch
- Gehirnerschütterung
- Photophobie
Andere Studien-ID-Nummern
- 2023H0291
Plan für individuelle Teilnehmerdaten (IPD)
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Klinische Studien zur Patienten mit traumatischer Hirnverletzung (TBI).
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Kessler FoundationInstituto Vocacional Enrique Díaz de León A.C., Guadalajara, MexicoRekrutierungTBI (Traumatic Brain Injury) oder MS (Multiple Sklerose)Vereinigte Staaten, Spanien