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NCT07328867Completed

Combined Effects of Dual-task and Perturbation Based Training on Balance and Cognition in Stroke Patients

Source: ClinicalTrials.gov · Last updated 9 Jan 2026

Brief summary (registry, in English)

This study aims to evaluate the Combined Effects of Dual-task and Perturbation Baesd Training on Balance and Cognition in Stroke Patients. Stroke is an acute cerebrovascular disorder that can impair cognitive, motor, and balanace abilites. Stroke is the second largest cause of death and disability globally. According tp studies, people who have had a stroke are more likely to fall than others who are same age and gender. PBBT is known as artificially induced balance training technique that can mimics the loss of balance that can occur naturally in freal life. Reduction in falls has been reported broadly by the use of perturbation based balance training. Current study will be and RCT on 33 participants based on the inclusion critieria. Participants will be randomly and equally divided into two groups; group B receiving Perturbation Based Training Alone and Group A receiving Dual-task and Perturbation Based Balance Training. The treatment will be given for 40 minutes, 3 days a week for 6 consecutive weeks. The assessment will be conducted at baseline, for cognition by Montreal Cognitive Assessment Scale (MoCA), for initial treadmill speed 10 Meter Walk Test (10MWT), for balance by Berg Balance Scale (BBS), and for fall riak by Fall Efficacy Scale (FES). Final assessment will be conducted after 6 weeks.

Status (registry)
Completed
Study type
Interventional
Enrollment
33 (actual)
First submitted
29 Dec 2025
Start date
14 Jun 2025
Primary completion date
26 Sept 2025
Lead sponsor
Foundation University Islamabad
Diseases
Stroke
NCT number
NCT07328867

What you commit to

  • Study type: Interventional
  • Participants enrolled: 33
  • From 14 Jun 2025 to the primary completion date, 26 Sept 2025
  • 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

  • Patient with sinificant co morbidties or secondary complications including orthopedic or rheumatological disorders were excluded
  • Patients with severe cognitive impairment or dementia
  • Patients with epilepsy or pacemaker

Other

  • Apraxia or hemi-neglect
  • Participants with body weight \>100kg
  • Participants with significant visual or hearing impairments
  • Participants with peripheral or central neuropathies that could impair balance

Who the study is looking for

  • No limitation of genders.
  • Age between 25-80 years
  • Participants diagnosed with chronic stroke
  • Participants being able to walk with or without walking aid independently or under supervision
  • Participants with impaired balance as indicated by a score of \<=41 on BBS
  • Participants with Montreal Cognitive Assessment Score \<26

Age in the registry: 25 years to 80 years · 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
Foundation University College of Physical Therapy
Coordinator of this site? Confirm its status
IslamabadPakistanUnknown status

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