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Clinical Trials/CTRI/2024/07/070441
CTRI/2024/07/070441CompletedNot Applicable

Influence of cognitive fatigue on dual task performance in healthy elderly individuals.

Mansi Tawari1 site in 1 country62 target enrollmentStarted: July 25, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
62
Locations
1
Primary Endpoint
Timed Up and Go Test

Study Overview

Brief Summary

  1. Participants will be recruited through snowball method from community outreach and healthcare facilities.

  2. Pre-screening assessments will be conducted to ensure eligibility based on inclusion and exclusion criteria.

  3. Informed consent will be obtained from each participant.

  4. Single task performance (Timed up and go test and n-back test) and dual task performance using TUG-NBT will be assessed. 1 practice trail will be given for both the tasks.

  5. Participants will undergo cognitive fatigue induction through a task.

  6. While the test is being carried out, the number of their responses said out loud will be recorded.

  7. Subjective reports of cognitive fatigue will be collected through Numeric Pain Rating Scale (NPRS).

  8. Single task and Dual Task performance will be assessed after induction of fatigue.

  9. The scores will be recorded and analysis will be done using appropriate statistical methods. Dual task cost will be calculated.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
60.00 Year(s) to 95.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •Age group 60 years & above
  • •Able to walk 3-meter distance with or without assistive device
  • •Have a score of 26 or higher on the Montreal Cognitive Assessment Scale.
  • •(No cognitive impairment)
  • •Able to follow commands.
  • •Able to read, understand and interpret Hindi or Marathi or English.
  • •Are educationally 8th grade pass.
  • •Willing to participate in the study.

Exclusion Criteria

  • •Uncorrected vision/ auditory impairments.
  • •Presence of diagnosed neurological or psychiatric disorders affecting cognitive function.
  • •History of recent major medical events or surgeries in the last 6 months.
  • •Severe sensory impairments affecting assessment participation.
  • •Current use of medications known to significantly influence cognitive performance.
  • •Pain on NPRS for any body part less than 4 or any orthopaedic condition, Lower limb fracture in last 6 months or any deformities that would affect walking ability.

Outcomes

Primary Outcomes

Timed Up and Go Test

Time Frame: Baseline

Secondary Outcomes

  • Montreal Cognitive Assessment (MOCA)(Baseline)
  • N-Back Test(Baseline)

Investigators

Sponsor
Mansi Tawari
Sponsor Class
Other [Self funded]
Responsible Party
Principal Investigator
Principal Investigator

Dr Atiya Shaikh PT

D.E.S Brijlal Jindal College of Physiotherapy

Study Sites (1)

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