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Active, not recruitingNCT07899372Updated Oct 27, 2026

EFFECTS OF AN OUTDOOR MAT PILATES PROGRAM ON NEUROPHYSIOLOGICAL INDICATORS OF ELDERLY INDIVIDUALS WITH MILD COGNITIVE IMPAIRMENT

An interventional study of Mat Pilates outdoor and Mat pilates closed environment in Cognition Disorders, sponsored by Letícia Maria Da Silva. Active, not recruiting at 1 site in Brazil. Open to participants aged 60 Years and older. Per ClinicalTrials.gov, last updated 2026-10-27.

Sponsored by Letícia Maria Da Silva · Not applicable, Interventional, and Treatment

Updated Oct 27, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
60 Years and older
Sex
All
01

Study summary

Introduction: As individuals age, the quality of cognitive function becomes an increasingly important topic. Elderly people, naturally, due to the aging process, may experience a reduction in cognitive function. Through the Pilates Method, greater cognitive performance can be generated, related to concentration and reasoning. Objectives: to evaluate the effects of practicing Mat Pilates outdoors on the neurophysiological parameters of elderly people with mild cognitive impairment. Materials and Methods: This is a randomized clinical trial study. Initially, the participants will be evaluated and the MoCA neurocognitive test will be applied. Before starting the Mat Pilates protocol, participants will undergo neurophysiological analysis, using electroencephalogram. Participants will undergo a group Mat Pilates protocol in the open air, lasting 60 minutes, which will be developed on two days during the week, on non-consecutive days. For each exercise, a series of 10 to 12 repetitions will be performed for each exercise, with a total duration of 6 weeks. At the end of the care protocol, participants will be reassessed

Read the detailed description

Introduction: As individuals age, the quality of cognitive function becomes an increasingly important topic. Elderly people, naturally, due to the aging process, may experience a reduction in cognitive function. Through the Pilates Method, greater cognitive performance can be generated, related to concentration and reasoning. Objectives: to evaluate the effects of practicing Mat Pilates outdoors on the neurophysiological parameters of elderly people with mild cognitive impairment. Materials and Methods: This is a randomized clinical trial study. Initially, the participants will be evaluated and the MoCA neurocognitive test will be applied. Before starting the Mat Pilates protocol, participants will undergo neurophysiological analysis, using electroencephalogram. Participants will undergo a group Mat Pilates protocol in the open air, lasting 60 minutes, which will be developed on two days during the week, on non-consecutive days. For each exercise, a series of 10 to 12 repetitions will be performed for each exercise, with a total duration of 6 weeks. At the end of the care protocol, participants will be reassessed

02

Conditions studied

  • Cognition Disorders

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03

In context

Cognition Disorders

399 studies on the registry are indexed under Cognition Disorders; 74 are open to participants now.

This study's planned enrollment of 40 is below the median of 66 across 272 interventional studies indexed under Cognition Disorders.

Browse Cognition Disorders studies →

Lead sponsor

This is the only study on the registry with Letícia Maria Da Silva as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

People of both sexes, 60 years of age or older, who have not been diagnosed with dementia. Those with a MOCA score between 18 and 25, which indicates mild cognitive impairment, will be included. Those who can attend Pilates sessions regularly, have not had surgery in the last six months, and have no restrictions recommended by their doctor.

Exclusion criteria

Exclusion Criteria:

People with any degenerative neurological condition, people with a history of traumatic brain injury with loss of consciousness, use of central nervous system depressant medications, major depression and epilepsy will be excluded from this research.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    outdoor environment

    Other: Mat Pilates outdoor

  • Active comparator
    closed environment

    Other: Mat pilates closed environment

Interventions

  • OtherMat Pilates outdoor

    Participants will undergo a 60-minute group Mat Pilates protocol outdoors, which will be performed on two non-consecutive days during the week. For each exercise, sets of 10 to 12 repetitions will be performed, lasting a total of 6 weeks. The exercises will follow the following order: preparation exercises, mobility exercises, strengthening exercises, and relaxation exercises, all of which will be associated with breathing.

  • OtherMat pilates closed environment

    Participants will undergo a 60-minute group Mat Pilates protocol, which will be performed on two non-consecutive days during the week. For each exercise, sets of 10 to 12 repetitions will be performed, lasting a total of 6 weeks. The exercises will follow the following order: preparation exercises, mobility exercises, strengthening exercises, and relaxation exercises, all of which will be associated with breathing.

06

What researchers measure

Primary outcomes

  1. Microstate analysis

    (1) The average duration for which a given microstate remains stable, (2) the frequency of occurrence of each microstate, regardless of its individual duration, (3) the fraction of the total recording time during which a given microstate is dominant (i.e., coverage), and (4) the global variance explained by each microstate.

    Time frame: After 6 weeks.

Secondary outcomes

  1. cognitive function screening

    Memory, attention, concentration, working memory, executive functions such as planning and organization, visuospatial abilities, language, and orientation to time and place will be assessed.

    Time frame: After 6 weeks.

07

Study locations

1 site
  • UFPB
    João Pessoa, Paraíba 58051-900, Brazil
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 27, 2026
Show all 1 update
  1. Oct 27, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07899372
Lead sponsor
Letícia Maria Da Silva
Collaborators
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.
Responsible party
Letícia Maria Da Silva (DOCTORAL STUDENT, Federal University of Paraíba) — Sponsor-investigator
First posted
Oct 27, 2026
Start date
Mar 1, 2026
Primary completion
Dec 2027 (estimated)
Completion
Apr 2028 (estimated)
Last update
Oct 27, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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