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ट्रायल रडार AI
क्लिनिकल ट्रायल NCT07489092 के लिए ICU Acquired Weakness (ICUAW) वर्तमान में भर्ती जारी है। सभी विवरणों के लिए क्लिनिकल ट्रायल रडार कार्ड दृश्य और AI खोज उपकरण देखें, या यहाँ कुछ भी पूछें।
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कार्ड दृश्य
खोज पर वापस जाएँ

Feasibility of a Digital Rehabilitation Platform in Patients After ICU Discharge 70

भर्ती जारी
चिकित्सा परीक्षण का विवरण मुख्य रूप से अंग्रेजी में उपलब्ध है। हालाँकि, ट्रायल रडार AI मदद कर सकता है! बस 'अध्ययन समझाएं' पर क्लिक करें और अपनी चुनी हुई भाषा में परीक्षण की जानकारी देखें और चर्चा करें।
क्लिनिकल ट्रायल NCT07489092 एक हस्तक्रियात्मक चिकित्सकीय अध्ययन है जो ICU Acquired Weakness (ICUAW) से जुड़ा हुआ है। परीक्षण वर्तमान में भर्ती जारी चल रहा है। इसकी शुरुआत 2 फ़रवरी 2026 को हुई थी, और इसमें कुल 70 प्रतिभागियों के नामांकन की योजना है। आसन मेडिकल सेंटर इस परीक्षण का नेतृत्व कर रहे हैं और इसके 31 दिसंबर 2026 तक पूरा होने की उम्मीद है। ClinicalTrials.gov वेबसाइट पर यह जानकारी 23 मार्च 2026 को अंतिम बार अपडेट की गई थी।
संक्षिप्त सारांश
This study aims to evaluate the feasibility, usability, and clinical effectiveness of a digital rehabilitation platform in adult patients discharged from the intensive care unit (ICU). Adult patients aged 19 years or older who stayed in the ICU for more than 48 hours and are capable of using a smartphone will be enrolled from two tertiary hospitals in South Korea.

Participants will receive individualized rehabilitat...

और दिखाएँ
विस्तृत विवरण
This is a prospective cohort clinical study designed to evaluate the feasibility, usability, and clinical effectiveness of a digital rehabilitation platform in adult patients discharged from the intensive care unit (ICU).

Study Population Eligible participants are adult patients aged 19 years or older who were admitted to the ICU for more than 48 hours at Seoul Asan Medical Center or Seoul National University Bundan...

और दिखाएँ
आधिकारिक शीर्षक

Feasibility of a Digital Rehabilitation Platform in Patients After ICU Discharge

स्वास्थ्य स्थितियां
ICU Acquired Weakness (ICUAW)
अन्य अध्ययन आईडी
  • 2026-0021
NCT नंबर
NCT07489092
अध्ययन प्रारंभ तिथि (वास्तविक)
2026-02-02
अंतिम अद्यतन प्रकाशित
2026-03-23
अध्ययन की समाप्ति तिथि (अनुमानित)
2026-12-31
नामांकन (अनुमानित)
70
अध्ययन प्रकार
हस्तक्रियात्मक
चरण
निर्दिष्ट नहीं
स्थिति
भर्ती जारी
प्रमुख शब्द
Intensive Care Unit Acquired weakness
Digital Therapeutics
प्राथमिक उद्देश्य
उपचार
डिज़ाइन आवंटन
निर्दिष्ट नहीं
हस्तक्षेप मॉडल
एकल समूह
अंधकरण
कोई नहीं (खुला लेबल)
समूह/हस्तक्षेप
प्रतिभागी समूह/शाखाहस्तक्षेप/उपचार
प्रयोगात्मकDigital Rehabilitation Group
Digital Rehabilitation Group
The Tuntun Rehabilitation Assistant is a smartphone-based digital rehabilitation platform designed for patients discharged from the intensive care unit. Rehabilitation sessions are conducted once daily, with each session lasting up to 30 minutes. During the initial five sessions, a researcher assists participants in performing the intervention in the hospital room. Thereafter, participants independently perform the p...और दिखाएँ
प्राथमिक परिणाम माप
परिणाम मापमाप विवरणसमय सीमा
Medical Research Council Sum Score (MRC-SS)
Summation score of muscle strength based on MRC scale. Unit of Measure: Sum score (0 to 60, where a higher score indicates better overall muscle strength.)
From enrollment to the end of treatment at 2 weeks
Functional Ambulatory Category (FAC)
Measurement of the level of ambulation and assistance required. Unit of Measure: FAC score (0 to 5, where a higher score indicates greater walking independence.)
From enrollment to the end of treatment at 2 weeks
Mini-Mental State Examination (MMSE)
Cognitive function assessment using the MMSE tool. Unit of Measure: MMSE score (0 to 30, where a higher score indicates better cognitive function.)
From enrollment to the end of treatment at 2 weeks
EQ-5D-5L
Assessment of patient-reported quality of life using the EQ-5D-5L questionnaire, which includes five dimensions (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression), each rated on a 5-level scale. Responses were converted to a utility index score. Unit of Measure: Utility score (0 to 1).
From enrollment to the end of treatment at 2 weeks
EQ-5D VAS
Assessment of patient-reported quality of life using the EQ-5D visual analog scale (VAS), where participants rate their overall health on a scale from 0 (worst imaginable health) to 100 (best imaginable health). Unit of Measure: VAS score (0 to 100).
From enrollment to the end of treatment at 2 weeks
SLR time
Assessment of straight leg raise (SLR) repetitions over 60 seconds and static holding ability. Unit of Measure: time (seconds) (For time: A higher value indicates better static endurance.)
From enrollment to the end of treatment at 2 weeks
SLR count
Assessment of straight leg raise (SLR) repetitions performed within 60 seconds. Unit of Measure: Count (repetitions) (For count: A higher value indicates better performance.)
From enrollment to the end of treatment at 2 weeks
Short Physical Performance Battery (SPPB) Total Score
Assessment of lower extremity physical performance using the Short Physical Performance Battery (SPPB), which includes balance tests, gait speed, and repeated chair stand tests. Scores range from 0 to 12, with higher scores indicating better physical performance. Unit of Measure: Total score (0 to 12).
From enrollment to the end of treatment at 2 weeks
भागीदारी सहायक
पात्रता मानदंड

अध्ययन के लिए पात्र आयु
वयस्क, वृद्ध वयस्क
अध्ययन के लिए न्यूनतम आयु
19 Years
अध्ययन के लिए पात्र लिंग
सभी
  • Age 19 years or older.
  • Admission to the intensive care unit (ICU) for more than 48 hours.
  • Hospitalization at Asan Medical Center or Seoul National University Bundang Hospital.
  • Discharge from the ICU at the time of enrollment.
  • Ownership of a smartphone and ability to operate a digital rehabilitation platform.
  • Ability to understand the study procedures and provide voluntary written informed consent.

  • Medical conditions that contraindicate participation in rehabilitation exercise, as determined by the attending physician.
  • Severe cognitive impairment or communication difficulties that interfere with understanding or following study instructions.
  • Unstable medical conditions requiring ongoing intensive medical treatment.
  • Inability to use a smartphone or digital platform independently.
  • Refusal to participate or withdrawal of informed consent.
Asan Medical Center logoआसन मेडिकल सेंटर152 सक्रिय क्लिनिकल ट्रायल्स खोजे जाने के लिए
अध्ययन उत्तरदायी पक्ष
Won Kim, मुख्य अन्वेषक, Associate Professor, Asan Medical Center
अध्ययन केंद्रीय संपर्क
संपर्क: Won Kim, Associate professor, 82+02-3010-1694, [email protected]
1 1 देशों में अध्ययन स्थान
Asan Medical Center, Seoul, South Korea
Won Kim, संपर्क, +82-02-3010-1694, [email protected]
भर्ती जारी