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TMS AND BOTULINUM TOXIN IN POST-STROKE UPPER LIMB SPASTICITY (TMS)

29 maj 2026 uppdaterad av: Asya ÖZCAN KAVCI

COMPARISON OF CLINICAL OUTCOMES ASSOCIATED WITH DIFFERENT TRANSCRANIAL MAGNETIC STIMULATION PROTOCOLS COMBINED WITH BOTULINUM TOXIN-A INJECTION IN POST-STROKE UPPER LIMB SPASTICITY

Post-stroke upper limb spasticity is an important condition that negatively affects motor recovery, upper limb functions, and activities of daily living. Multimodal treatment approaches are recommended in the management of spasticity. In recent years, the effects of transcranial magnetic stimulation (TMS) on upper limb functions and spasticity have been investigated. However, the clinical effects of different TMS protocols combined with botulinum toxin-A (BTX-A) treatment and which protocol may be more effective remain unclear. The aim of this observational study is to compare the clinical effects of different TMS protocols in patients with post-stroke upper limb spasticity receiving BTX-A treatment and to evaluate the most appropriate TMS protocol.

Studieöversikt

Detaljerad beskrivning

As part of the study, patients who received botulinum toxin type A (BTX-A) injections for upper extremity spasticity following stroke were evaluated using different TMS protocols. All patients received a standard conventional physical therapy program. TMS sessions were conducted using an inhibitory protocol, with a total of 10 sessions administered to the contralateral hemisphere at least 3 days per week. Clinical evaluations were performed at baseline, at 1 month, and at 3 months. Thus, the early and long-term clinical outcomes of treatment were investigated. Spasticity was assessed using the Modified Ashworth Scale (MAS), motor improvement using the Brunnstrom staging system, upper extremity motor function using the Fugl-Meyer Assessment, and upper extremity use in activities of daily living using the Motor Activity Log-28 (MAL-28). Additionally, patients' anxiety and depression levels were measured using the Hospital Anxiety and Depression Scale (HADS).

Studietyp

Interventionell

Inskrivning (Faktisk)

39

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Ankara
      • Ankara, Ankara, Turkiet (Türkiye), 06010
        • Ankara Etlik City Hospital, Physical Medicine and Rehabilitation Clinic

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Nej

Beskrivning

Inclusion Criteria:

  • Diagnosis of stroke (ischemic or hemorrhagic)
  • Time since stroke onset between 3 and 24 months
  • Age between 18 and 80 years
  • Upper extremity motor recovery at Brunnstrom Stages 3-5
  • Spasticity in the elbow, wrist, or finger flexor muscle groups of the upper extremity with a Modified Ashworth Scale (MAS) score between +1 and 3
  • Receipt of botulinum toxin-A injection to the affected upper extremity within the previous week

Exclusion Criteria:

  • History of epileptic seizures, epileptiform EEG findings, increased seizure risk, or use of antiepileptic medication
  • Presence of implanted metallic or electronic devices (e.g., cardiac pacemaker, intrathecal baclofen pump)
  • Pregnancy or lactation
  • Presence of neurological disorders other than stroke
  • History of cranial surgery
  • Orthopedic conditions or previous orthopedic surgery limiting upper extremity movement
  • Severe upper extremity spasticity (MAS >3) or presence of contracture
  • Uncontrolled hypertension, advanced heart failure (NYHA Class III-IV), chronic obstructive pulmonary disease (COPD), active infection, severe hepatic failure, or severe renal failure
  • History of malignancy
  • Severe cognitive impairment (Mini-Mental State Examination score <24)
  • Severe aphasia or communication disorder that would interfere with participation in the study
  • Botulinum toxin injection administered to the upper extremity in a separate treatment session within the previous 3 months
  • Any change in medication type or dosage within the previous month for oral medications used in the management of spasticity

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Dubbel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: rTMS Group
Participants received botulinum toxin-A treatment, conventional physical therapy, and repetitive transcranial magnetic stimulation (rTMS) using an inhibitory stimulation protocol.
Repetitive transcranial magnetic stimulation (rTMS) was applied to the contralateral hemisphere using an inhibitory stimulation protocol. Treatment was administered in 10 sessions, at least 3 days per week, in combination with botulinum toxin-A injections and conventional physical therapy.
Sham Comparator: Sham rTMS Group
Participants received botulinum toxin-A treatment, conventional physical therapy, and sham repetitive transcranial magnetic stimulation (sham rTMS). The sham procedure was designed to mimic active stimulation without delivering therapeutic stimulation.
Sham repetitive transcranial magnetic stimulation (sham rTMS) was administered using procedures designed to mimic active stimulation without delivering therapeutic magnetic stimulation. Treatment was provided in combination with botulinum toxin-A injections and conventional physical therapy.
Experimentell: cTBS Group
Participants received botulinum toxin-A treatment, conventional physical therapy, and continuous theta burst stimulation (cTBS) using an inhibitory stimulation protocol.
Continuous theta burst stimulation (cTBS) was applied to the contralateral hemisphere using an inhibitory stimulation protocol. Treatment was administered in 10 sessions, at least 3 days per week, in combination with botulinum toxin-A injections and conventional physical therapy.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in Spasticity Assessed by Modified Ashworth Scale (MAS)
Tidsram: Baseline, 1 Month, and 3 Months
Spasticity severity was assessed using the Modified Ashworth Scale.
Baseline, 1 Month, and 3 Months

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in Motor Recovery Assessed by Brunnstrom Staging
Tidsram: Baseline, 1 Month, and 3 Months
Motor recovery of the upper extremity and hand was assessed using Brunnstrom staging.
Baseline, 1 Month, and 3 Months
Change in Upper Extremity Motor Function Assessed by Fugl-Meyer Assessment
Tidsram: Baseline, 1 Month, and 3 Months
Upper extremity motor function was assessed using the Fugl-Meyer Assessment.
Baseline, 1 Month, and 3 Months
Change in Upper Extremity Use Assessed by Motor Activity Log-28
Tidsram: Baseline, 1 Month, and 3 Months
The frequency and quality of upper extremity use in daily activities were assessed using the Motor Activity Log-28.
Baseline, 1 Month, and 3 Months
Change in Anxiety and Depression Levels Assessed by Hospital Anxiety and Depression Scale
Tidsram: Baseline, 1 Month, and 3 Months
Anxiety and depression levels were assessed using the Hospital Anxiety and Depression Scale.
Baseline, 1 Month, and 3 Months

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Damla CANKURTARAN, Associate Professor, MD, Ankara Etlik City Hospital, Department of Physical Medicine and Rehabilitation

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

20 januari 2025

Primärt slutförande (Faktisk)

26 maj 2026

Avslutad studie (Faktisk)

26 maj 2026

Studieregistreringsdatum

Först inskickad

29 maj 2026

Först inskickad som uppfyllde QC-kriterierna

29 maj 2026

Första postat (Faktisk)

3 juni 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

3 juni 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

29 maj 2026

Senast verifierad

1 maj 2026

Mer information

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IPD-planbeskrivning

Individual participant data will not be shared due to privacy and confidentiality considerations.

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