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Neuromuscular electrical stimulation to combat cognitive aging in people with spinal cord injury: protocol for a single case experimental design study.
Vints, Wouter A J; Levin, Oron; van Griensven, Martijn; Vlaeyen, Johan W S; Masiulis, Nerijus; Verbunt, Jeanine; van Laake-Geelen, Charlotte C M.
Affiliation
  • Vints WAJ; Department of Health Promotion and Rehabilitation, Lithuanian Sports University, Sporto Str. 6, Kaunas, LT-44221, Lithuania. w.vints@maastrichtuniversity.nl.
  • Levin O; Department of Rehabilitation Medicine Research School CAPHRI, Maastricht University, P.O. Box 616, Maastricht, 6200 MD, The Netherlands. w.vints@maastrichtuniversity.nl.
  • van Griensven M; Centre of Expertise in Rehabilitation and Audiology, Adelante Zorggroep, P.O. Box 88, Hoensbroek, 6430 AB, The Netherlands. w.vints@maastrichtuniversity.nl.
  • Vlaeyen JWS; Department of Health Promotion and Rehabilitation, Lithuanian Sports University, Sporto Str. 6, Kaunas, LT-44221, Lithuania.
  • Masiulis N; Movement Control & Neuroplasticity Research Group, Group Biomedical Sciences, KU Leuven, Tervuursevest 101, Heverlee, 3001, Belgium.
  • Verbunt J; Department of Cell Biology-Inspired Tissue Engineering, MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, P.O. Box 616, Maastricht, 6200 MD, The Netherlands.
  • van Laake-Geelen CCM; Experimental Health Psychology, Faculty of Psychology and Neuroscience, Maastricht University, Maastricht, Netherlands.
BMC Neurol ; 24(1): 197, 2024 Jun 11.
Article in En | MEDLINE | ID: mdl-38862912
ABSTRACT

INTRODUCTION:

Individuals with spinal cord injury (SCI) can experience accelerated cognitive aging. Myokines (factors released from muscle cells during contractions), such as brain-derived neurotrophic factor (BDNF), are thought to have beneficial effects on cognition. Neuromuscular electrical stimulation (NMES) was shown to elicit a large release of myokines. However, the effects of NMES on cognitive function have not been studied.

OBJECTIVE:

To present the study protocol for a clinical trial evaluating the effects of NMES aimed at improving cognition and BDNF.

METHODS:

A replicated randomized three-phases single-case experimental design (SCED) with sequential multiple baseline time series and a single-armed prospective trial will be conducted with 15 adults with chronic SCI (> 12 months after injury) above L1 neurological level undergoing 30-min quadriceps NMES, 3 days per week for 12 weeks. MAIN STUDY ENDPOINTS Primary endpoint is cognitive performance (assessed by a smartphone test) conducted three times per week during the baseline phase with random duration of 3 to 8 weeks, the intervention phase of 12 weeks, and the follow-up phase of 3 weeks after a no measurement rest period of 12 weeks. Secondary endpoints are changes in BDNF levels and cognitive performance measured before the baseline period, before and after intervention and after a 12 weeks follow-up.

CONCLUSION:

This will be the first study investigating the effects of 12 weeks NMES on both cognition and BDNF levels in individuals with SCI. The SCED results provide information on individual treatment effect courses which may direct future research. TRIAL REGISTRATION ClinicalTrials.gov (NCT05822297, 12/01/2023).
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Full text: 1 Database: MEDLINE Main subject: Spinal Cord Injuries / Electric Stimulation Therapy / Brain-Derived Neurotrophic Factor Limits: Adult / Female / Humans / Male / Middle aged Language: En Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Main subject: Spinal Cord Injuries / Electric Stimulation Therapy / Brain-Derived Neurotrophic Factor Limits: Adult / Female / Humans / Male / Middle aged Language: En Year: 2024 Type: Article