ClinicalTrials.gg
Not yet recruitingNCT07819266CPTUpdated Sep 14, 2026

Cognitive Postural Training for Hemineglect Patient After Stroke

An interventional study of Cognitive postural training and Conventional physical therapy program in Hemineglect After Stroke, sponsored by Ahram Canadian University. Not yet recruiting at 1 site in Egypt. Open to participants aged 45 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-09-14.

Sponsored by Ahram Canadian University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
42
Allocation
Randomized
Ages
45 Years to 65 Years
Sex
All
01

Study summary

This randomized controlled trial investigates the effect of Cognitive Postural Training (CPT) on postural stability and cognitive function in patients with hemispatial neglect following stroke. Participants will be randomly assigned to receive either Cognitive Postural Training combined with conventional balance training or conventional balance training alone. Training will be provided three times per week for four weeks. The effects of the intervention on cognitive function, hemispatial neglect, postural stability, balance, and functional independence will be evaluated.

02

Conditions studied

  • Hemineglect After Stroke

Browse trials for

03

In context

Stroke

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

This study's planned enrollment of 42 is below the median of 49 across 6,024 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Ahram Canadian University is the lead sponsor of 71 studies on the registry; 42 are open to participants now.

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

04

Who can participate

Ages eligible
45 Years to 65 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

  • Patients from both genders with hemispatial neglect due to first ever right cerebral hemisphere stroke (ischemic or hemorrhagic).
  • Age of participants ranged from 45 to 65 years.
  • Mild to moderate degree of unilateral spatial neglect according to Catherine Bergego scale.(Appendix VI)
  • The duration of the stroke was at least six months.
  • ranged from 18.5 - 30 Kg/m2.
  • score more than 21 (Nasreddine, et al., 2005).
  • Mini mental state examination score between 20 and 24 (Li, et al., 2016).
  • Grade of spasticity less than two according to Modified Ashworth Scale (Harb and kishner 2022).
  • Berg balance scale score less than 45 (Miranda-Cantellops, et al., 2022).
  • Muscle power of lower limbs 3 or more

Exclusion criteria

Exclusion Criteria:

  • 21) Other brain injuries/illnesses, psychiatric, sever cognitive impairment, severe sensory or proprioceptive loss.

    22) Other causes of cognitive dysfunction. 23) Severe apraxia, severe aphasia. 24) Drugs that affect balance or cognition 25) Ankle disorders (e.g.sprain), vestibular disorder 26) ophthalmic disorders, homonymous hemianopsia 27) Progressive neurological disease (e.g., dementia)

Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

MMSE and MoCA

Short tests of memory and thinking, each scored out of 30. Lower scores suggest more difficulty; criteria give a range, either to include people with memory problems or to leave them out.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
42 participants (estimated)

Study arms

  • Experimental
    Cognitive postural training group

    Other: Cognitive postural training · Other: Conventional physical therapy program

  • Active comparator
    Conventional physical therapy program group

    Other: Conventional physical therapy program

Interventions

  • OtherCognitive postural training

    CPT consisted of simultaneous performance of cognitive tasks and postural control activities to challenge cognitive-motor integration and postural stability. Cognitive tasks included verbal fluency (e.g., naming animals), mental sequencing (e.g., reciting the months of the year in reverse order), and route-description tasks. Training was progressively performed in different postural positions, including supine, sitting, sit-to-stand, and standing, according to the participant's abilities and level of postural control.

  • OtherConventional physical therapy program

    conventional balance training focuses on improving postural control, balance, and functional mobility. Training included static and dynamic balance exercises performed in different postural positions, including sitting, sit-to-stand, and standing. Exercises were progressed according to the participant's functional ability and balance performance and included weight-shifting activities, maintaining and changing the base of support, and functional balance activities.

06

What researchers measure

Primary outcomes

  1. Overall Stability Index (OSI) - Biodex Balance System

    Time frame: Once at enrollment once at the end of treatment that will last 4 weeks

  2. Psotural stability- Berg Balance Score

    Time frame: Once at enrollment once at end of treatment that will last for 4 weeks

Secondary outcomes

  1. Cognitive Function - Montreal Cognitive Assessment (MoCA)

    Time frame: Once at enrollment once at end of treatment that will last for 4 weeks

  2. Global Cognitive Function - Mini-Mental State Examination (MMSE)

    Time frame: Once at enrollment once at end of treatment that will last for 4 weeks

  3. Hemispatial Neglect - Star Cancellation Test

    Time frame: Once at enrollment once at the end of treatment that will last 4 weeks

  4. Hemispatial Neglect - Catherine Bergego Scale (CBS)

    Time frame: Once at enrollment once at the end of treatment that will last 4 weeks

  5. Functional Independence - Barthel Index (BI)

    Time frame: Once at enrollment once at the end of treatment that will last 4 weeks

07

Study locations

1 site
  • The out patient clinic Faculty of physicaltherapy Cairo university
    Giza, Egypt
08

References and documents

Individual participant data

Plan to share: Yes

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07819266
Lead sponsor
Ahram Canadian University
Responsible party
Alaa Elbaroudy (Teaching assistant, Ahram Canadian University) — Principal investigator
First posted
Sep 14, 2026
Start date
Sep 15, 2026 (estimated)
Primary completion
Oct 2026 (estimated)
Completion
Nov 2026 (estimated)
Last update
Sep 14, 2026

Study contacts

Alaa M Elbaroudy
Contact
Alaaelbaroudy76@gmail.com
201061547547

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 not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion