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Enhanced Motor Recovery Using Serotonergic Agents in Stroke

26 december 2016 bijgewerkt door: T. George Hornby, Shirley Ryan AbilityLab

The information derived from this study will be critical to establishing appropriate rehabilitative interventions post-stroke. In particular, traditional use of pharmacological agents to alter motor function post-stroke is directed primarily at reducing the "positive" signs following upper motor neuron lesion, in particular spasticity, or enhanced, velocity-dependent stretch reflex responses to imposed stretch. While pharmacological management of spasticity certainly suppresses clinical and quantitative measures of hypertonia, there is little improvement in functional performance. In contrast, preliminary data on the administration of 5HT agents following neurological injury indicates an increase in motor performance (Pariente 2001) and recovery (Dam 1996), despite an increase in spastic motor activity (Stolp-Smith 1999; see Preliminary Data below). Understanding methods to maximize function following stroke despite potential, short-term increases in spastic motor activity may improve therapeutic intervention strategies. The general objective of this study is therefore to:

  1. quantify the effects of short-term SSRI administration on voluntary and spastic motor behaviors in individuals with chronic spastic hemiparesis,
  2. identify the changes in impairments and functional recovery of walking ability during BWSTT with the presence or absence of SSRIs.

Studie Overzicht

Toestand

Voltooid

Gedetailleerde beschrijving

Walking ability post-stroke is characterized primarily by reduced walking speed and endurance and impaired postural stability which limits functional and societal reintegration. Decreased over ground walking speed is a result of decreased cadence, decreased stride length and increased non-paretic single limb stance duration. Mechanisms underlying reduced velocity are thought to include weakness in the paretic limb, particular hip flexor and plantarflexor strength, but may also be linked spastic motor behaviors and loss of inter- and intra-limb coordination. Rehabilitation efforts to improve strength and muscle coordination patterns during hemiparetic gait may improve gait quality and velocity and therefore improve performance of activities of daily living.

To improve gait performance and functional outcomes following neurological injury, rehabilitation efforts have focused on re-establishing normal walking patterns . Towards this end, the use of body-weight supported treadmill training (BWSTT) has demonstrated significant improvement in walking capability in individuals post-stroke and spinal cord injury . By supporting a portion of a subject's body weight over a treadmill and providing manual facilitation from therapists, previous research has demonstrated improvements in temporal-spatial gait patterns, including gait velocity , endurance (Macko 2005), balance , and symmetry. Importantly, the changes in impairments and functional limitations observed with intensive BWSTT are often greater than that achieved during conventional or lower intensity physical therapy. Given these benefits, particularly in those who require substantial walking assistance following stroke various robotic locomotor retraining devices have been developed to facilitate practice of "kinematically correct" stepping patterns to improve the consistency and duration of treadmill training.

While the changes observed following BWSTT are statistically and functionally significant, it remains unclear is the benefits of such intensive training paradigms are optimized. Specifically, across many larger studies in subjects with chronic stroke (i.e., those > 6 mo. post-injury), mean increases in walking speed range between 0.09 m/s to 0.15 m/s following 1-6 mos. of training. Even in current trials investigating changes in over ground walking speed in robotic- vs. therapist-assisted BWSTT, mean improvements over at least 18 subjects in each group vary from 0.07 to 0.13 m/s, respectively (please see Preliminary work: Pilot Study 1). While again statistically significant, such changes represent an approximate 10% improvement in gait speed as compared to healthy adults (Perry 1992).

To enhance the benefits of intensive BWSTT, many investigators continue to search for combined interventions to augment recovery. One potential adjunct that has received attention is the use of pharmacological agents. For example, anti-spastic medications (e.g., benzodiazepine, baclofen, tizanidine) have been used for decades (to reduce the presence or severity of involuntary, spastic reflexes in patients with stroke. Spasticity has traditionally been thought to be a primary limitation to functional mobility post-stroke, although this premise has been questioned recently . Indeed, many pharmacological agents are effective in reducing spastic motor behaviors although evidence for improvements in function following use of these agents post-stroke is limited. In addition, some evidence suggests that these agents reduce maximal voluntary strength and can impair learning of motor tasks.

New evidence has emerged of a potentially powerful role of excitatory or facilitative modulatory agents in the treatment of motor impairments post-stroke. Based primarily on evidence from experimentally induced lesions in mammals, the application of monoaminergic (i.e., serotonin [5HT] and norepinephrine [NE]) agents excite vs. depress spinal or cortical excitability have gained momentum. In individuals post-stroke, for example, the use of amphetamines (directed primarily through NE pathways) had generated substantial interest as an adjunct to physical therapy interventions, although recent data may suggest no benefit from this agent. Further, the use of amphetamines may enhance the risk of cerebral or coronary vascular disease, which is already compromised in this patient population, and therefore limit the use of these agents in clinical practice.

In contrast, 5HT agents have also been shown to enhance spinal and/or cortical excitability, and may accelerate locomotor recovery following neurological injury when appropriate physical interventions are provided . In humans post-stroke, one study has demonstrated enhanced motor performance and cortical activity following a single dose of SSRIs. In another study of sub-acute stroke, SSRIs and not selective NE reuptake inhibitors improved function during inpatient rehabilitation. Interestingly, a small case report indicates a strong increase in spasticity following use of 5HTergic anti-depressive agents, indicating that both spinal and cortical excitability may contribute to altered motor function. Such findings have been replicated here (please see Preliminary work: Pilot Study I, although certainly require further assessment.

While the above findings are preliminary, two important questions arise. First, if both spastic and voluntary lower extremity activity are simultaneously altered following administration of commonly used anti-depressive medications, how does the relation between these variable alter motor function? Echoing tothers, how important is the prevalence of spasticity to impaired motor function post-stroke? Secondly, can the increased excitability of both spinal and cortical systems following SSRI accelerate motor recovery and the effectiveness of intensive physical rehabilitation strategies, as shown in reduced preparations? Such data are important for health care professionals treating individuals with neurological injury to: A) understand the previously unknown modulation in reflex or voluntary function following a seemingly innocuous agent; and, to B) provide the optimal neural excitability to accelerate motor performance and recovery post-injury.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

30

Fase

  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Illinois
      • Chicago, Illinois, Verenigde Staten, 60611
        • Rehabilitation Institute of Chicago

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar tot 75 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  • unilateral supratentorial stroke
  • MMSE > 22
  • > 6 months stroke duration
  • < 0.9 m/s gait speed overground

Exclusion Criteria:

  • lower extremity contracture
  • osteoporosis
  • Cardiovascular/metabolic/respiratory instability
  • previous central/peripheral nerve injury
  • concurrent medications interacting with SSRIs

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Crossover-opdracht
  • Masker: Verviervoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: SSRI
SSRI alone or with training
SSRI alone or with training
Andere namen:
  • escitalopram
Placebo-vergelijker: Placebo
Placebo alone or with training
Placebo alone or with training

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Peak treadmill speed
Tijdsspanne: 4 weeks
4 weeks

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
overground walking speed
Tijdsspanne: 4 weeks
4 weeks

Andere uitkomstmaten

Uitkomstmaat
Tijdsspanne
gait kinematics
Tijdsspanne: 4 weeks
4 weeks
EMG activity
Tijdsspanne: 4 weeks
4 weeks

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Thomas G Hornby, Shirley Ryan Abilitylab

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 december 2004

Primaire voltooiing (Werkelijk)

1 januari 2012

Studie voltooiing (Werkelijk)

1 januari 2012

Studieregistratiedata

Eerst ingediend

14 december 2012

Eerst ingediend dat voldeed aan de QC-criteria

14 december 2012

Eerst geplaatst (Schatting)

18 december 2012

Updates van studierecords

Laatste update geplaatst (Schatting)

28 december 2016

Laatste update ingediend die voldeed aan QC-criteria

26 december 2016

Laatst geverifieerd

1 december 2012

Meer informatie

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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