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ENHANCING PHYSICAL and COGNITIVE EFFICIENCY in INDIVIDUALS AT RISK of DEMENTIA USING WHOLE-BODY ELECTROMYOSTIMULATION

ENHANCING PHYSICAL and COGNITIVE EFFICIENCY in ELDERLY INDIVIDUALS AT RISK of DEMENTIA USING WHOLE-BODY ELECTROMYOSTIMULATION

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06669598
Enrollment
61
Registered
2024-11-01
Start date
2024-01-07
Completion date
2024-06-30
Last updated
2024-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mild Cognitive Impairment

Keywords

WB-Electromyostimulation; EMS; electrical muscle stimulation; muscle strength; neurodegenerative disease; cardiovascular training

Brief summary

This study aimed to evaluate the effectiveness of twelve weeks whole-body electrical muscle stimulation combined with aerobic exercises.

Detailed description

This study aimed to evaluate the effectiveness of twelve weeks of WB-EMS (whole-body electrical muscle stimulation at 35Hz and 350 μs) combined with aerobic exercises on a treadmill and rowing machine, in improving physical and cognitive performance in older adults, both healthy and at risk of dementia. The results were compared with those obtained from the same training without WB-EMS.

Interventions

The ETG group underwent in two 20-minute training sessions per week (12 weeks), with 72 hours of rest between sessions. Each session included aerobic activities such as rowing and treadmill exercises, combined with supervised WB-EMS stimulation. This stimu-lation utilised a rectangular waveform at 35 Hz, 350 μs, with continuous pulse dura-tion

BEHAVIORALcontrol group

The CON group underwent three weekly training sessions for twelve weeks, con-sisting of 20 minutes of aerobic activity, performed on a treadmill and rowing machine, without the WB-EMS superimposition.

Sponsors

University of Molise
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
55 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* age from 55 to 85 years; * no simultaneous participation in any type of supervised physical activity; * Sedentary lifestyle

Exclusion criteria

* mini-mental state examination (MMSE) score of less than 24; * inability to walk for 6 min without assistance; * the presence of a medical condition influencing the cognitive and/or motor functions; * the presence of any counter indication for the utilisation of EMS, such as cardiovascular diseases, stents, cardiac pacemakers, and diabetes mellitus, verified by medical certification.

Design outcomes

Primary

MeasureTime frame
30-second arm curl testAt the end of 12 weeks
30-second sit-to-stand testAt the end of 12 weeks
hand grip strength testAt the end of 12 weeks
6-minute walking testAt the end of 12 weeks
8-foot up and go testAt the end of 12 weeks
Chair Sit and Reach TestAt the end of 12 weeks
Soda Pop TestAt the end of 12 weeks
Tinetti Balance and Gait TestAt the end of 12 weeks
Mini-Mental State Examination (MMSE)At the end of 12 weeks
Rey's Auditory Verbal Learning Test (RAVLT)At the end of 12 weeks
Stroop Colour and Word Interference Test (SCWT)At the end of 12 weeks
Trail Making Test (TMT)At the end of 12 weeks
Attentional Matrices TestAt the end of 12 weeks
Prose recall test ( babcock)At the end of 12 weeks
Frontal Assessment battery (FAB)At the end of 12 weeks

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026