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NCT05592249Completed

The Effect of Dual Tasks on ADL in Stroke

The Effect of Different Dual Task Practices on Activities of Daily Living in Stroke Individuals

Source: ClinicalTrials.gov · Last updated 21 Feb 2024

Brief summary (registry, in English)

The aim of this study is to investigate the effectiveness of different dual-task practices on activities of daily living in stroke patients. The sample size was calculated as 18 people for each group and 36 people in total, with a 20% drop out. MC (Motor - Cognitive) group will receive 60 minutes motor - cognitive dual task intervention 5 day per week for 6 weeks in clinic. MM (Motor - Motor) group will receive 60 minutes motor - motor dual task intervention 5 day per week for 6 weeks in clinic. As the primary outcomes in the study; Modified Barthel Index will be used to evaluate basic activities of daily living, Nottingham Extended Activities of Daily Living Index designed specifically for stroke to evaluate instrumental activities of daily living, and Stroke Impact Scale 3.0 to evaluate participation in activities of daily living. As secondary outcomes; 10 Meter Walk Test will be used for functional mobility assessment, Timed Up and Go Test and Berg Balance Scale will be used for balance assessment, Motor Activity Log-28 will be used to assess upper extremity functions, and Montreal Cognitive Assessment Test will be used for cognitive status assessment.

Status (registry)
Completed
Study type
Interventional
Enrollment
29 (actual)
First submitted
20 Oct 2022
Start date
26 Dec 2022
Primary completion date
20 Dec 2023
Lead sponsor
Istanbul University - Cerrahpasa
Diseases
Stroke
NCT number
NCT05592249

What you commit to

  • Study type: Interventional
  • Participants enrolled: 29
  • From 26 Dec 2022 to the primary completion date, 20 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Presence of additional neurological disease

Other

  • Having orthopedic problems that may prevent walking
  • Presence of apraxia
  • The patient has a hearing loss that cannot understand the commands given
  • To have a score below 30 on the Beck Depression Scale

Who the study is looking for

  • To be diagnosed with stroke by a specialist physician
  • Modified Rankin Score ≤ 3 with moderate or mild disability
  • To score 21 and above on the Montreal Cognitive Assessment Test
  • Be over 18 years old
  • Volunteering to participate in the study

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
İstanbul University-Cerrahpaşa
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.