- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07588932
Relying on Pharmacotherapy to Improve Motor Gains in Chronic Stroke Survivors
Relying on Pharmacotherapy to Improve Motor Gains of Robot-Assisted Upper-Extremity Rehabilitation in Chronic Stroke Survivors
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
The overall objective of the proposed study is to assess the viability of a pharmacotherapy combining Telmisartan, Cilostazol IR, and Metformin ER to affect the motor gains achieved via robot-assisted (RA) upper-extremity (UE) rehabilitation in stroke survivors. The hypothesis underlying the study design is that concomitant administration of Telmisartan, Cilostazol IR, and Metformin ER (herein referred to as "the proposed pharmacotherapy") leads to enhancing motor and non-motor gains observed in stroke survivors in response to RA UE rehabilitation. Participants will take these medications either once a day (QD) or twice a day (BID) as described in the protocol.
To test this hypothesis, we plan to accomplish the following primary and secondary aims.
Primary Aims:
- 1 To determine if administration of the proposed pharmacotherapy in combination with RA UE rehabilitation leads to greater improvements in UE motor impairment than previously observed in clinical trials relying on RA UE rehabilitation alone.
- 2 To evaluate potential adverse events when using the proposed pharmacotherapy in combination with RA UE rehabilitation.
Secondary Aim:
#1 To determine if the proposed pharmacotherapy in combination with RA UE rehabilitation improves UE functional ability, health related quality of life, and cognition.
Exploratory Aims:
- 1 To determine the association between response to the proposed pharmacotherapy and serum-based biomarkers collected at baseline (i.e., evaluation session prior to training), during the first training session (beginning and end of the session), during the last training session (beginning and end of the session), and during the 3-month follow-up evaluation session.
- 2 To evaluate the retention of motor and cognitive gains at 1-month post-intervention.
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Tidlig fase 1
Kontakter og lokationer
Studiekontakt
- Navn: Madison Costa, OT
- Telefonnummer: 617-952-6388
- E-mail: mcosta11@mgb.org
Undersøgelse Kontakt Backup
- Navn: Erin Foley, OT
- Telefonnummer: 617-952-6388
- E-mail: efoley14@mgb.org
Studiesteder
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Massachusetts
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Charlestown, Massachusetts, Forenede Stater, 02129
- Spaulding Rehabilitation Hospital
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Kontakt:
- Paolo Bonato, PhD
- Telefonnummer: 617-952-6388
- E-mail: pbonato@mgh.harvard.edu
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Kontakt:
- Federico De Carlo, MS
- Telefonnummer: 617-952-6388
- E-mail: fdecarlo@mgb.org
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Adults between 21 and 80 years of age.
- History of ischemic stroke.
- Stroke occurred at least six months prior to recruitment.
- Moderate to severe UE impairment (FMA-UE score between 15 and 40)
- MMSE score >=20 and being able to safely follow three-step commands.
Exclusion Criteria:
- Contraindications to the pharmacotherapy (e.g., heart failure, known medication reaction or interactions with ongoing medication regimen).
- Taking dual antiplatelet therapy (e.g., Aspirin+Plavix) and/or other anticoagulation medications (e.g., Eliquis, coumadin) that cannot safely be modified or discontinued (as determined by the participant's primary care physician or by the medical monitor).
- Clinically significant somnolence and/or depression that would hinder active participation in motor training sessions.
- Taking any medication that the study physician determines to have a significant drug-drug interaction with Telmisartan, Cilostazol, and/or Metformin.
- Taking Telmisartan, Cilostazol, and/or Metformin in a dose that is different from the one used in the study and that cannot be adjusted to match the study dose (as determined by the participant's primary care physician or by the medical monitor).
- Taking medications with equivalent clinical effect (e.g., BP control) to Telmisartan, Cilostazol, and/or Metformin and that cannot be replaced by Telmisartan, Cilostazol, and/or Metformin (as determined by the participant's primary care physician or by the medical monitor).
- A body mass index (BMI) below 25 (as the proposed pharmacotherapy could cause hypoglycemia in participants with normal-low BMI).
- Severe musculoskeletal pathology or recent fractures affecting the impaired UE that would prevent safe use of the rehabilitation robotic system.
- Previous diagnosis of neurological diseases other than stroke that would have a negative impact on the response to the rehabilitation intervention (e.g., severe dystonia affecting the UE) or would prevent safe participation in RA UE training (e.g., uncontrolled seizures).
- Moderate to severe disability due to migraines as determined using the Migraine Disability Assessment test (score > 10).
- Severe spasticity (Modified Ashworth Scale for spasticity ≥ 3 for UE muscles) that would prevent safe use of the robotic system utilized during training.
- Undergoing Botox treatment for pain/spasticity related to the affected upper extremity, in the 4 months prior to enrollment or during the study period.
- Cerebellar and/or hemorrhagic stroke.
- Severe aphasia limiting the ability to express needs or discomfort verbally or non-verbally.
- Visual impairments that would prevent proper use of interactive on-screen games during RA UE training.
- Severe hemispatial neglect as assessed using the Line Bisection Test (missed lines >2).
- Severely impaired trunk control that would prevent sitting safely on a chair without arms.
- Individuals who present with the following on the impaired UE: open wounds, fragile skin, and under contact precautions due to an active infection.
- Participation in another therapy focused on the recovery of the impaired UE.
- Subjects with cardiac pacemakers, electronic pumps, or any other implanted medical devices that are not US-certified (and hence might be affected by the electromagnetic interference generated by the robot).
- Any condition that would prevent proper/safe use of the robotic system, such as proprioceptive deficits that impair the ability to process haptic or visual feedback, or unstable shoulder joint as assessed by physical examination.
- Current pregnancy.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Intervention
Participants will be instructed to take Telmisartan, Cilostazol IR (immediate release), and Metformin ER (extended release) (herein referred to as "proposed pharmacotherapy") while undergoing robot-assisted upper-extremity training.
Participants will take these medications either once a day (QD) or twice a day (BID) as described in the protocol.
|
Participants will be instructed to take the low dose of the proposed pharmacotherapy (i.e., Telmisartan 20mg QD, Metformin ER 500mg QD, Cilostazol IR 50mg QD) during week 1 and the full dose (i.e., Telmisartan 40mg QD, Metformin ER 500mg BID, Cilostazol IR 50mg BID) starting on week 2.
They will continue to take the full dose until completion of the six-week robot assessed upper extremity training period (week 3-8).
At the end of this period, they will be instructed to take the low dose of the proposed pharmacotherapy for two more weeks.
During the entire study, participants will be monitored for potential side-effects.
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Fugl-Meyer Assessment - Upper Extremity (FMA-UE)
Tidsramme: Will be assessed at baseline, at 8 weeks, and at the end of the 12-week study
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The FMA-UE is a widely used, standardized test that measures movement, coordination, and reflexes of the arm, wrist, and hand after a stroke.
Scores reflect the degree of motor impairment, with higher scores indicating better motor function (range 0-66).
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Will be assessed at baseline, at 8 weeks, and at the end of the 12-week study
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Action Research Arm Test (ARAT)
Tidsramme: Will be assessed at baseline, at 8 weeks, and at the end of the 12-week study.
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The ARAT is a standardized test of upper limb function after stroke.
It assesses the ability to grasp, grip, pinch, and move objects, with higher scores indicating better arm and hand function (range 0 to 57).
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Will be assessed at baseline, at 8 weeks, and at the end of the 12-week study.
|
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Stroke Impact Scale (SIS)
Tidsramme: Will be completed at baseline, at 8 weeks, and at the end of the 12-week study.
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The SIS is a self-reported questionnaire that measures how stroke has affected daily activities, mobility, communication, emotion, memory, and quality of life.
Higher scores reflect better function and well-being (range 0 to 100)
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Will be completed at baseline, at 8 weeks, and at the end of the 12-week study.
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Mini Mental State Exam (MMSE scale)
Tidsramme: Will be completed at baseline, at 8 weeks, and at the end of the 12-week study.
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An 11-question measure that tests five areas of cognitive function: orientation, registration, attention and calculation, recall, and language (range 0 to 30).
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Will be completed at baseline, at 8 weeks, and at the end of the 12-week study.
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Samarbejdspartnere og efterforskere
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Qing M Wang, MD, PhD, Spaulding Rehabilitation Hospital
Publikationer og nyttige links
Generelle publikationer
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- Veerbeek JM, Langbroek-Amersfoort AC, van Wegen EE, Meskers CG, Kwakkel G. Effects of Robot-Assisted Therapy for the Upper Limb After Stroke. Neurorehabil Neural Repair. 2017 Feb;31(2):107-121. doi: 10.1177/1545968316666957. Epub 2016 Sep 24.
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Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Cerebrovaskulære lidelser
- Hjernesygdomme
- Sygdomme i centralnervesystemet
- Sygdomme i nervesystemet
- Karsygdomme
- Hjerte-kar-sygdomme
- Slag
- Organiske kemikalier
- Heterocykliske forbindelser, 1-ring
- Heterocykliske forbindelser
- Benzimidazoler
- Heterocykliske forbindelser, 2-ring
- Heterocykliske forbindelser, smeltet ring
- Azoler
- Kulbrinter
- Kulbrinter, cyklisk
- Kulbrinter, aromatisk
- Benzenderivater
- Biguanides
- Guanidiner
- Amidiner
- Quinoliner
- Tetrazoler
- Biphenylforbindelser
- Telmisartan
- Cilostazol
- Metformin
Andre undersøgelses-id-numre
- 2024P003711
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
IPD-delingstidsramme
IPD-delingsadgangskriterier
IPD-deling Understøttende informationstype
- STUDY_PROTOCOL
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