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Not yet recruiting NCT07668245

Effectiveness of Attention Focus Training on Attention and Quality of Life in Stroke

No phase Interventional Stroke

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Exercise, Conventional.
Who it may be relevant to
Registry conditions: Stroke. Basic parameters: up to 55 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Pakistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This RCT will determine the effects of attention focus training which is a comprehensive intervention to improve cognitive outcomes. Attention is one of the major cognitive outcome and problems with attention can deteriorate the quality of life of people suffering from stroke. Intervention will be provided for 4 weeks. Outcomes will be assessed at baseline and after provision of intervention.

Interventions

  • Other Exercise
    Focused attention (auditory target detection), Sustained attention (letter cancellation), Selective attention (cancellation with distractors), Alternating attention (number-letter switching)
  • Other Conventional
    Positioning and bed mobility, sitting balance training, standing training

Primary outcome measures

  • Test of Everyday Attention [Time frame: Baseline and post 4 weeks of intervention]
  • Stroke Impact Scale [Time frame: Baseline and post 4 weeks of intervention]

Eligibility criteria

Inclusion criteria

  • Participants diagnosed with stroke
  • Able to ambulate at least with assistance
  • Medically stable

Exclusion criteria

  • Severe cognitive impairment (MMSE < 24)
  • Pre-existing dementia
  • Visual/hearing impairment

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Pakistan · 1 center
  • Shifa Tameer-e-Millat University — Islamabad

Identifiers

NCT: NCT07668245 · 026-26

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗