ClinicalTrials.gg
CompletedNCT07100899Updated Aug 3, 2025

Effects of Dual Task Training Versus Task-specific Training on Lower Limb Function, Trunk Control and Balance in Chronic Stroke Patients: A Randomized Controlled Trial

An interventional study of Dual task training and Task-specific training in Stroke, sponsored by Ahmed Alshimy. Completed at 1 site in Egypt. Open to participants aged 45 Years to 55 Years. Per ClinicalTrials.gov, last updated 2025-08-03.

Sponsored by Ahmed Alshimy · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
45
Allocation
Randomized
Ages
45 Years to 55 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 93 studies in Stroke with a site in Egypt — 25 open to participants now, 29 under way, 2 of them phase 3. Stroke · Egypt.

Enrollment
32nd of 75
45 · median 42
Started
2025
with 21 others
No phase
66 of 93
18 open now
Registered
67th of 93
by date
Lead sponsor
4 of 93
Ahmed Alshimy

Among the 93 studies in Stroke with a site in Egypt, this one is the 32nd largest by enrollment of the 75 interventional ones that give a count, is one of 22 that started in 2025, is one of 66 with no phase, and was the 67th registered.

Stroke

8,255 studies on the registry are indexed under Stroke; 2,056 are open to participants now.

This study's enrollment of 45 is close to the median of 49 across 6,024 interventional studies indexed under Stroke.

Browse Stroke studies →

Open to participants now

25 of the 93 studies in Stroke with a site in Egypt are open now, in 1 country. Each count lists the studies.

All 25 open studies →

Who these studies take

Of the 1,415 Stroke studies recruiting now, 697 (49%) set no upper age limit and 280 (20%) stop at 75 or younger; 77 take children under 18; 196 take healthy volunteers.

This study: 45 Years to 55 Years · all sexes · no healthy volunteers.

The full table on the hub →
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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 93 studies in Stroke with a site in Egypt, or all of them as a file.
02

Study summary

One of the leading causes of disability among the elderly is stroke. After a stroke, it is highly usual for lower extremity function, balance and trunk control to be compromised. After a stroke, trunk control is a crucial early predictor of functional recovery. Following a stroke, proximal trunk control is necessary for distal limb movement control, balance, and functional capacity.

Read the detailed description

Forty-five chronic stroke patients, ages 45 to 55, were divided into three equal groups for this randomized controlled study: GA consisted of 15 patients, GB of 15 patients, and GC of 15 patients each. Group A (the study group) received dual motor task training in addition to the selected physiotherapy program, Group B (the study group) received task-oriented training in addition to the selected physiotherapy program, and Group C only received the selected physiotherapy program for 12 weeks. All groups received treatment three times a week for twelve weeks, with each session lasting sixty minutes. The Trunk Impairment Scale (TIS), Functional Reach Test (FRT), Biodex Balance System (BBS), and Fugl Meyer Lower Extremity (FM-LE) were used to evaluate each of the three groups pre and post treatments.

03

Conditions studied

  • Stroke

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Keywords

  • Stroke
  • dual task training
  • task-specific training
  • lower extremity
  • balance
  • trunk control
04

Who can participate

Ages eligible
45 Years to 55 Years
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

  • 45 chronic stroke patients between the ages of 45 and 55 who were of both sexes, had been ill with stroke for more than six months to a year, had received at least nine years of education, had a score on the Berg balance scale between 41 and less than 45, and had cognitive functions greater than 26 on the MOCA scale were included in this study

Exclusion criteria

Exclusion Criteria:

  • Patients who had any neurological condition that affected balance other than stroke (such as inner ear, vestibular, or cerebellar dysfunction), communication disorders, uncontrolled hypertension, diabetes, or unstable angina, hearing or vision issues, or respiratory disorders were not allowed to participate.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Double (Participant, Investigator)
Enrollment
45 participants (actual)

Study arms

  • Experimental
    Group A

    received dual motor task training in addition to the selected physiotherapy program, three times a week for twelve weeks, with each session lasting sixty minutes.

    Other: Dual task training · Other: Selected physiotherapy program

  • Experimental
    Group B

    received task-oriented training in addition to the selected physiotherapy program, three times a week for twelve weeks, with each session lasting sixty minutes.

    Other: Task-specific training · Other: Selected physiotherapy program

  • Other
    Group C

    only received the selected physiotherapy program, three times a week for twelve weeks, with each session lasting sixty minutes.

    Other: Selected physiotherapy program

Interventions

  • OtherDual task training

    Dual motor task training for 30 minutes. The dual motor training was divided into two phases. The first part involved a single task condition in which the stroke patient was instructed to stand up from a seated position at a self-selected speed without the use of upper limb assistance. Cognitive and physical tasks, is the second part of training. In addition to a 30-minute selected physiotherapy program.

  • OtherTask-specific training

    Began with a highchair before switching to a low one. In addition to a 30-minute selected physiotherapy program.

  • OtherSelected physiotherapy program

    Consisting of trunk control, trunk stabilization, balance training and lower extremity strengthening exercises (primarily for the hip adductors and abductors) for 60 minutes.

06

What researchers measure

Primary outcomes

  1. Trunk impairment scale

    It assesses trunk coordination skills as well as static and dynamic balance while seated

    Time frame: 4 weeks

  2. Functional Reach test

    This one-item exam is intended to serve as a rapid screening tool for balance issues

    Time frame: 4 weeks

  3. Biodex Balance System

    Used to evaluate balance

    Time frame: 4 weeks

  4. Fugl-Meyer lower extremity

    This test is designed to evaluate lower extremity motor and sensory impairment after a stroke

    Time frame: 4 weeks

07

Study locations

1 site
  • Al Ryada University for Science and Technology
    Sadat, Menoufia, Egypt
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jun 2025 to primary completion in Jul 2025, 1 month.

Of 3,108 non-industry interventional studies with no phase under Stroke, half reached primary completion within 23 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 46. This study's 1 month is below that.

Counting every sponsor, half of 3,252 studies reached it within 23 months; a quarter within 10 and three quarters within 46.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 28, 2025
First posted
Aug 3, 2025
StartActual
Jun 5, 2025
Primary completionActual
Jul 5, 2025
CompletionActual
Jul 10, 2025
Last update
Aug 3, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 3, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07100899
Lead sponsor
Ahmed Alshimy
Responsible party
Ahmed Alshimy (Lecturer of Physical Therapy for Neurology and it's Surgery, AlRyada University for Science & Technology) — Sponsor-investigator
First posted
Aug 3, 2025
Start date
Jun 5, 2025
Primary completion
Jul 5, 2025
Completion
Jul 10, 2025
Last update
Aug 3, 2025

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 completed, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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