Long-Term Clinical, Health Economic, and Process Evaluation of Intensive Technology-Integrated Motor Rehabilitation in Chronic Neurological Conditions (INTeRAcT-bis)
A legfontosabb adatok
- Hol
- Herentals és Leuven (Belgium)Mind a 2 helyszín megnézése
AI-kivonat: kiket keres a vizsgálat
A vizsgálat saját részvételi feltételeiből. Gép olvasta ki az oldalon álló regiszterszövegből, ezért tévedhet. Hogy ki vehet részt, azt a lenti regiszterszöveg és a vizsgálat csapata dönti el.
A vizsgálat olyan felnőtteket keres, akik agyvérzésen vagy gerincvelő-sérülésen estek át, otthon élnek, és részt vettek az első INTeRAcT vizsgálatban. Egy második, 3 hetes intenzív rehabilitációs időszakot tesztel.
- Életkor
- 18 évnél idősebb
- Nem
- Minden nem csatlakozhat.
- A betegség stádiuma
- Legalább 3 hónapja diagnosztizált agyi érkatasztrófa (sztrók), vagy gerincvelő-sérülés, amelyet az ASIA skálán A, B, C vagy D értékre soroltak. Egy vagy mindkét kar vagy láb gyengesége.
- Korábbi kezelés
- Részt kellett venni az első INTeRAcT vizsgálatban. A kórházból vagy a rehabilitációs központból való távozás óta legalább 3 hónapnak el kell telnie. Otthon kell élni.
A részvétel fő kizáró okai
- Más idegrendszeri vagy mozgásszervi betegség, amely befolyásolhatja a vizsgálatot
- Nem tudja megkezdeni a mozdulatokat a gravitáció ellenében a karokban és a lábakban
- Súlyos látás-, kommunikációs, gondolkodási vagy nyelvi problémák
- Terhes vagy szoptató nők
- Bármilyen állapot, amely a vizsgáló szerint veszélyeztetné a biztonságot vagy akadályozná a vizsgálat követését
Gépi kiolvasás: 2026. november 12.
Helyszínek itt: Belgium
- AZ HerentalsHerentals, BelgiumNo longer taking part
- KU LeuvenLeuven, BelgiumNo longer taking part
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakA vizsgálat adatai
- Ki végzi
- KU Leuven
- Azonosító
- NCT07912320
- A regiszteradat frissítve
- 2026. november 3.
- Eredeti leírás
Rehabilitation remains important in the chronic phase after stroke or spinal cord injury, as meaningful improvements may still be achieved through intensive, goal-directed, and personalized training. INTeRAcT-bis is a follow-up study of the original INTeRAcT program, which consisted of a 3-week intensive rehabilitation intervention (90 therapy hours) combining conventional therapy, goal-directed training, self-management, and advanced rehabilitation technologies. The study has two main objectives: (1) to evaluate the long-term clinical and health economic effects of the original INTeRAcT program, and (2) to assess the clinical effects and implementation of a second intensive rehabilitation period ("boost"). Participants receive a personalized 3-week rehabilitation program targeting upper and/or lower limb impairments based on their individual goals. In addition to clinical and health economic outcomes, the study examines participant experiences and implementation factors to support a broader implementation of intensive rehabilitation in the future.A teljes eredeti leírásKevesebb
Rehabilitation remains important in the chronic phase after stroke or spinal cord injury, as meaningful improvements may still be achieved through intensive, goal-directed, and personalized training. INTeRAcT-bis is a follow-up study of the original INTeRAcT program, which consisted of a 3-week intensive rehabilitation intervention (90 therapy hours) combining conventional therapy, goal-directed training, self-management, and advanced rehabilitation technologies. The study has two main objectives: (1) to evaluate the long-term clinical and health economic effects of the original INTeRAcT program, and (2) to assess the clinical effects and implementation of a second intensive rehabilitation period ("boost"). Participants receive a personalized 3-week rehabilitation program targeting upper and/or lower limb impairments based on their individual goals. In addition to clinical and health economic outcomes, the study examines participant experiences and implementation factors to support a broader implementation of intensive rehabilitation in the future.
Bevonási feltételek: Voluntary written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedures; A diagnosis of central neurological disease, made by a specialist. Conditions may include stroke or spinal cord injury:; Stroke:; Participants must have received a diagnosis of stroke and have been diagnosed at least 3 months ago; Participants who are diagnosed for the second time, but returned to normal functioning after the first stroke diagnosis (Barthel Index > 85/100), and the affected side is the same as the first stroke; SCI: Participants have a rating A, B, C or D on the American Spinal Injury Association (ASIA) measurement scale, which refers to patients with complete or incomplete impairment. All levels of SCI can be included, if there is a clear patient need linked to the upper and/or lower extremities; At least 3 months post-discharge from hospital/rehabilitation center, living at home; Had a normal functional state prior to the pathology: a pre-pathology Barthel Index > 85/100; Unilateral or bilateral weakness of the affected upper or lower limbs (No maximum score in all affected limbs = motricity index: score 5 on 3/3 segments); Having the clinical opportunity to engage in exercise therapy with available technology, assessed by a specialist (under supervision of an MD); Age of > 18 years; Sufficient cognitive ability to understand the therapy exercises and give informed consent, assessed by a specialist (under supervision of an MD); Having participated in the first INTeRAcT study.
Kizáró feltételek: Having other neurological or musculoskeletal conditions that may affect the protocol, assessed by a specialist (under supervision of an MD); Severe visual impairment, communication, cognitive, and language formation problems that would prevent the intervention and measurement process, assessed by a specialist (under supervision of an MD); Any disorder, which in the investigator's opinion might compromise the participant's safety or compliance with the CIP; No ability to initiate movements against gravity in the upper and lower limbs; A female who is pregnant or breastfeeding.