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CompletedNCT07027787HDUpdated Jun 19, 2025

Incentive Training Role in Treatment of Hand Dexterity in Patients With Stroke

An interventional study of Standard Physical Therapy for Hand Dexterity in Stroke Patients and Rehacom Attention Training + Physical Therapy in Stroke, sponsored by South Valley University. Completed at 1 site in Egypt. Open to male participants aged 45 Years to 60 Years. Per ClinicalTrials.gov, last updated 2025-06-19.

Sponsored by South Valley University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 1 month after the study started (first participant enrolled May 2023, registered Jun 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
45 Years to 60 Years
Sex
Male
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Study summary

Attention and hand dexterity are interdependent, with deficits in one often worsening the other. Post-stroke, reduced attention impairs hand dexterity, hindering daily activities, while poor hand function further limits attentional focus. Despite progress in rehabilitation, strategies addressing both remain limited. Purpose: This study explored the impact of incentive-based attention training on hand dexterity in stroke patients.

Read the detailed description

Forty male patients with hemorrhagic infarction stroke, aged 45-60 years, were randomized into two equal groups. The control group (Group A, n=20) underwent hand dexterity exercises for 60 minutes per session, while the intervention group (Group B, n=20) received a combination of 30 minutes of hand dexterity exercises and 30 minutes of attention training using the Rehacom system. Both groups completed three training sessions per week for eight weeks (24 sessions). Outcomes were assessed pre- and post-training using the Mindful Attention Awareness Scale (MAAS), Hand Grip Dynamometer, Rehacom system, and Purdue Pegboard Test (PPBT).

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Conditions studied

  • Stroke

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Keywords

  • Incentive training
  • Attention
  • Hand dexterity
  • stroke
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In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.

This study's enrollment of 40 is below the median of 50 across 5,369 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

South Valley University is the lead sponsor of 147 studies on the registry; 46 are open to participants now.

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

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Who can participate

Ages eligible
45 Years to 60 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  1. ) Male patients diagnosed with chronic hemorrhagic infarction stroke
  2. ) Stroke diagnosis confirmed through CT or MRI scans
  3. ) Referred by a neurologist or neurosurgeon
  4. ) Right-handed
  5. ) Aged between 45 and 60 years
  6. ) Stroke duration ranging from 6 months to 1 year
  7. ) Mini-Mental State Examination (MMSE) score of 24 or higher
  8. ) Montreal Cognitive Assessment (MoCA) score above 21, indicating no significant cognitive impairment
  9. ) Mild spasticity (Grade 1 or 1+ on the Modified Ashworth Scale)
  10. ) Brunnstrom's Stage 4 or 5 of recovery

Exclusion criteria

Exclusion Criteria:

  1. ) Unstable medical conditions (e.g., diabetes mellitus or hypertension)
  2. ) Language deficits that could impair cooperation
  3. ) Blindness or deafness
  4. ) Severe cognitive impairments affecting task performance
  5. ) Presence of brain tumors
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Care provider)
Enrollment
40 participants (actual)

Study arms

  • Active comparator
    Standard Physical Therapy for Hand Dexterity in Stroke Patients

    Standard physical therapy program for stroke patients targeting hand dexterity. Conducted 3 times/week for 8 weeks (60 min/session), exercises included wrist and forearm movements, object manipulation, ball gripping, and putty-based hand strengthening.

    Behavioral: Standard Physical Therapy for Hand Dexterity in Stroke Patients

  • Active comparator
    Rehacom Attention Training + Physical Therapy

    Combined intervention: 30 minutes of computerized attention training using the Rehacom system, followed by 30 minutes of standard hand dexterity physical therapy. Conducted 3 times/week for 8 weeks. Rehacom provided task-based cognitive training with visual, auditory, and performance feedback in a controlled lab setting.

    Behavioral: Rehacom Attention Training + Physical Therapy

Interventions

  • BehavioralStandard Physical Therapy for Hand Dexterity in Stroke Patients

    Standard physical therapy program for stroke patients targeting hand dexterity. Conducted 3 times/week for 8 weeks (60 min/session), exercises included wrist and forearm movements, object manipulation, ball gripping, and putty-based hand strengthening.

  • BehavioralRehacom Attention Training + Physical Therapy

    Combined intervention: 30 minutes of computerized attention training using the Rehacom system, followed by 30 minutes of standard hand dexterity physical therapy. Conducted 3 times/week for 8 weeks. Rehacom provided task-based cognitive training with visual, auditory, and performance feedback in a controlled lab setting.

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What researchers measure

Primary outcomes

  1. Hand dexterity assessment using the Purdue Pegboard Test (PPBT)

    The Purdue Pegboard Test (PPBT) is a timed neuropsychological assessment used to evaluate fine motor skills, finger dexterity, and bimanual coordination by measuring how quickly a person can place small pegs into holes using one or both hands.

    Time frame: 8 Weeks

  2. Hand grip dynamometer (JAMAR)

    The JAMAR hand dynamometer is a reliable and widely used tool for measuring grip strength, featuring a peak-hold needle and adjustable handle settings to accommodate different hand sizes and ensure consistent, accurate readings.

    Time frame: 8 weeks

Secondary outcomes

  1. Rehacom system

    The Rehacom system is a CE-certified, software-based cognitive rehabilitation tool that personalizes training and assessment in domains like attention, memory, and logic. This study utilizes its attention-concentration module to evaluate the cognitive performance of stroke patients through detailed reaction-time metrics and adaptive difficulty levels.

    Time frame: 8 Weeks

  2. The Mindful Attention Awareness Scale (MAAS)( 6 is high 6 , 1 is low)

    The MAAS (Mindful Attention Awareness Scale) is a 15-item self-report tool that measures an individual's open and receptive awareness of present-moment experiences, with strong psychometric validity and associations with emotional, behavioral, and health outcomes; it can be completed in under 5 minutes, with higher scores indicating greater mindfulness and lower scores reflecting more frequent mind-wandering or inattentiveness.

    Time frame: 8 Weeks

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Study locations

1 site
  • Cairo University Faculty of Physical Therapy
    Cairo, 11262, Egypt
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References and documents

Individual participant data

Plan to share: Yes — After approval can be shared

Supporting information: Study protocol

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 19, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07027787
Lead sponsor
South Valley University
Collaborators
Princess Nourah Bint Abdulrahman University, Keele University, Cairo University, Queen Margaret University, Delta University for Science and Technology, Misr University for Science and Technology
Responsible party
Omar Mohamed Kamel (researcher, South Valley University) — Principal investigator
First posted
Jun 19, 2025
Start date
May 1, 2023
Primary completion
Mar 31, 2024
Completion
Mar 31, 2024
Last update
Jun 19, 2025

Study contacts

Reem M Alwhaibi, master
study chair · College of Health and Rehabilitation Sciences, Princess Nourah bint Abdulrahman University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2025. You cannot join it, but the record below documents what was studied.

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