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ट्रायल रडार AI
क्लिनिकल ट्रायल NCT05716048 (CRUSH-IT) के लिए आघातजन्य मस्तिष्क चोट वर्तमान में भर्ती जारी है। सभी विवरणों के लिए क्लिनिकल ट्रायल रडार कार्ड दृश्य और AI खोज उपकरण देखें, या यहाँ कुछ भी पूछें।
एक परीक्षण फ़िल्टर मानदंडों से मेल खाता है
कार्ड दृश्य

Combinatory Rehabilitation Used for Substantially Helping Individuals With Traumatic Brain Injury (CRUSH-IT)

भर्ती जारी
चिकित्सा परीक्षण का विवरण मुख्य रूप से अंग्रेजी में उपलब्ध है। हालाँकि, ट्रायल रडार AI मदद कर सकता है! बस 'परीक्षण समझाएं' पर क्लिक करें और अपनी चुनी हुई भाषा में परीक्षण की जानकारी देखें और चर्चा करें।
क्लिनिकल परीक्षण NCT05716048 (CRUSH-IT) का मुख्य उद्देश्य उपचार का अध्ययन करना है। यह चिकित्सकीय अध्ययन आघातजन्य मस्तिष्क चोट से जुड़ा हुआ है और यह एक चरण I हस्तक्रियात्मक परीक्षण है। परीक्षण वर्तमान में भर्ती जारी चल रहा है। इसकी शुरुआत 21 अप्रैल 2023 को हुई थी, और इसमें कुल 60 प्रतिभागियों के नामांकन की योजना है। केसलर फाउंडेशन इस परीक्षण का नेतृत्व कर रहे हैं और इसके 28 फ़रवरी 2028 तक पूरा होने की उम्मीद है। ClinicalTrials.gov वेबसाइट पर यह जानकारी 4 सितंबर 2025 को अंतिम बार अपडेट की गई थी
संक्षिप्त सारांश
New learning and memory impairment (NLMI) is a common and devastating manifestation of TBI associated with substantial life burdens. Persons with moderate to severe TBI have shown improvement in NLM for prose material (e.g. story) as well as beneficial changes in default-mode network (DMN) activation during list-learning19 following treatment with the Kessler Foundation modified Story Memory Technique® (KF-mSMT®). Benefits, however, were moderate and did not yield downstream improvements in daily life. It is thus critical to examine other approaches to complement the KF-mSMT® for robustly managing NLMI in TBI. The proposed RCT will be the first to include aerobic exercise training (AET) as a highly-promising complement to the KF-mSMT® for robustly managing NLMI, examining impact on NLM, its neural correlates, and daily life in NLM impaired persons with moderate-to-severe TBI. We thus propose a two-arm, parallel group, double-blind RCT comparing the effects of the KF-mSMT+AET with the KF-mSMT+S/T (active control condition) on NLM (Aim 1), hippocampal MRI (Aim 2), and daily life outcomes (Aim 3). 60 NLM impaired persons with moderate-to-severe TBI will be randomized to one of 2 conditions (30 per condition). Each condition will take place 3 days per week for 12 weeks and will be supervised by KF personnel. Participants will be blinded as to the intent of the conditions. We will further explore baseline predictors of clinically meaningful changes in NLM for those completing the KF-mSMT + AET condition (Exploratory Aim 4). If successful, this trial will position combinatory KF-mSMT and AET within the clinician's arsenal for robustly managing NLMI in persons with TBI. By augmenting the effects of KF-mSMT with AET, this treatment aims to exert a powerful countermeasure to TBI-related NLMI, and ultimately help those with TBI-related NLMI return to the workforce, independently manage their everyday lives, and maintain optimal quality of life. Additionally, while rigorously designed to answer the scientific question of the relative benefit of AET with the KF-mSMT, the proposed study is will likely provide some level of benefit to all study participants.

If successful, this trial will provide Class I evidence of combined KF-mSMT and AET for rehabilitating NLMI in TBI, based on standards published for therapeutic trials by the American Academy of Neurology, thus positioning such an approach within the clinician's arsenal for robustly managing NLMI. By augmenting the effects of KF-mSMT with AET, we anticipate this treatment will ultimately help those with TBI-related NLMI return to the workforce, independently manage their everyday lives, and maintain optimal quality of life.

आधिकारिक शीर्षक

Randomized Controlled Trial of Combined Cognitive Rehabilitation and Exercise Training for Learning and Memory in Persons With Moderate to Severe Traumatic Brain Injury

चिकित्सीय स्थितियाँ
आघातजन्य मस्तिष्क चोट
अन्य अध्ययन आईडी
  • CRUSH-IT
  • R-1195-22
NCT नंबर
अध्ययन प्रारंभ तिथि (वास्तविक)
2023-04-21
अंतिम अद्यतन प्रकाशित
2025-09-04
अध्ययन की समाप्ति तिथि (अनुमानित)
2028-02-28
नामांकन (अनुमानित)
60
अध्ययन प्रकार
हस्तक्रियात्मक
चरण
चरण I
स्थिति
भर्ती जारी
प्राथमिक उद्देश्य
उपचार
डिज़ाइन आवंटन
यादृच्छिक
हस्तक्षेप मॉडल
समानांतर
अंधकरण
दोहरा अंध
समूह/हस्तक्षेप
प्रतिभागी समूह/हाथहस्तक्षेप/इलाज
प्रयोगात्मकKF-mSMT Plus Aerobic Exercise Training
Participants will undergo 12 weeks of supervised aerobic cycling exercise training. During the last 8 weeks of cycling exercise, participants will also undergo treatment with the Kessler Foundation modified Story Memory Technique as an approach for cognitive rehabilitation.
KF-MSMT Plus Aerobic Exercise Training
Participants will undergo this combinatory intervention 3 days per week for 12 weeks. The combined session duration will begin with 15 minutes and last up to 2 hours by the end of the 12th week
सक्रिय तुलना समूहKF-mSMT Plus Stretching Exercise Training
Participants will undergo 12 weeks of supervised stretching and toning exercise training. During the last 8 weeks of stretching exercise, participants will also undergo treatment with the Kessler Foundation modified Story Memory Technique as an approach for cognitive rehabilitation.
KF-MSMT Plus Stretching Exercise Training
Participants will undergo this combinatory intervention 3 days per week for 12 weeks. The combined session duration will begin with 15 minutes and last up to 2 hours by the end of the 12th week
प्राथमिक परिणाम माप
परिणाम मापमाप विवरणसमय सीमा
Change in California Verbal Learning Test-3 Performance
This is a test of new learning and memory
From 0 to 12 weeks
द्वितीयक परिणाम माप
परिणाम मापमाप विवरणसमय सीमा
Change in hippocampal volume
This involves a structural MRI scan wherein the volume of the bilateral hippocampi will be measured.
From 0 to 12 weeks
Change in hippocampal activation
This involves an fMRI list-learning task wherein activation of the hippocampus during encoding and recall will be measured
From 0 to 12 weeks
Change in hippocampal resting-state functional connectivity
This involves a resting-state fMRI paradigm wherein connectivity between the hippocampus and other brain regions that are important for learning and memory will be measured.
From 0 to 12 weeks
Change in Everyday Memory Simulations Performance
This multi-component test examines aspects of memory that are relevant to daily life.
From 0 to 12 weeks
पात्रता मानदंड

अध्ययन के लिए पात्र आयु
वयस्क, वृद्ध वयस्क
अध्ययन के लिए न्यूनतम आयु
18 Years
अध्ययन के लिए पात्र लिंग
सभी
  • Age between 18-65 to control for age related brain changes
  • Diagnosis of moderate-to-severe TBI based on TBIMS criteria at least one year prior to enrollment
  • Having no to low substance use / involvement (drug/alcohol) as documented via ASSIST
  • Being insufficiently physically active based on a Godin Leisure-Time Exercise Questionnaire Health Contribution Score of <14
  • Having a proficiency in the English language
  • Being right handed to control for brain organization
  • Having chronic medical conditions (e.g. diabetes) in addition to TBI will require approval to participate from a physician, consistent with PAR-Q+.
  • Having an in-tact ability to follow directions based on the Telephone Interview for Cognitive Status (TICS-M) (i.e., TICS-M scores of ≥18)
  • Demonstrating new learning and memory impairment based on Open-Trial Selective Reminding Task (OT-SRT) scores at least 1.5 standard deviations below healthy controls (8+ trials to reach criterion)

  • Regularly taking steroids & benzodiazapines to control for medications effects
  • Having a history of neurological disorders beyond TBI
  • Having a history of severe mental illness (e.g., schizophrenia, bipolar, severe major depression)
  • Having metal in the body, claustrophobia, and other risk factors that would make MRI scanning unsafe.
  • Having moderate or high risk for exercise training contraindications (e.g. diabetes), defined as ≥1 YES on pages 2-3 of the Physical Activity Readiness Questionnaire for Everyone (PAR-Q+)
  • Having significantly impaired vision by scotomas (corrected vision in worse eye worse than 20/60), diplopia, or nystagmus.
अध्ययन उत्तरदायी पक्ष
Brian Sandroff, मुख्य अन्वेषक, Senior Research Scientist, Kessler Foundation
अध्ययन केंद्रीय संपर्क
संपर्क: Nancy Moore, MA, 973-324.8450, [email protected]
1 1 देशों में अध्ययन स्थल

New Jersey

Kessler Foundation, West Orange, New Jersey, 07052, United States
Brian M Sandroff, PhD, संपर्क
भर्ती जारी