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A comparison between the effects of Task-Oriented Training combined with Bobath programme and Task-Oriented Training alone on the function of upper extremity in post-stroke hemiparesis patients

A comparison between the effects of Task-Oriented Training combined with Bobath programme and Task-Oriented Training alone on the function of upper extremity in post-stroke hemiparesis patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017051316680N4
Enrollment
16
Registered
2017-07-16
Start date
2017-06-05
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke. Cerebral palsy and other paralytic syndromes

Interventions

Intervention 1: The control group will receive Task-Oriented Training program alone for 60 min. Intervention 2: The intervention group will receive combination of Task-Oriented Training with Bobath pr
Rehabilitation
The control group will receive Task-Oriented Training program alone for 60 min.
The intervention group will receive combination of Task-Oriented Training with Bobath programfor 60 min: 30 min Bobath programme and 30 min Task-Oriented Training.

Sponsors

Vice Cancellor for Research of Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: first unilateral hemiparesis following stroke ranging between 2-12 months (sub-acute and chronic stage); MMSE more than 20; Motor recovery of hand Brunnstrom stages = 3; score of spasticity of the elbow flexors = 3 based on the Modified Ashworth Scale (MAS); they must have 45-70 years of age; score of Depression based on the Geriatric Depression Scale (GDS) = 8; and they do not receive any upper-limb rehabilitation programs during the participation in this study. Exclusion criteria: they have previous injury, disease, or contracture of the upper extremity; no sitting balance; any co-morbid neurological disease or condition such as multiple sclerosis, Parkinson disease, spinal cord injury, traumatic brain lesions, brain tumor, epilepsy, or dementia; and they have Hemineglect phenomena.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Upper limb function. Timepoint: Exactly before the treatment, in the six treatment session,and exactly after the treatment. Method of measurement: By Wolf Motor Function Test.;Strength of the hand. Timepoint: Exactly before the treatment, in the six treatment session,and exactly after the treatment. Method of measurement: by using Hand Strength Test.;Motor function of upper extremity. Timepoint: Exactly before the treatment, in the six treatment session,and exactly after the treatment. Method of measurement: By using Fugl Meyer Test.;Sitting balance. Timepoint: Exactly before the treatment, in the six treatment session,and exactly after the treatment. Method of measurement: By using Modified Functional Reach Test.

Secondary

MeasureTime frame
Activities of Daily Living. Timepoint: Exactly before the treatment, in the sixth treatment session,and exactly after the treatment. Method of measurement: By using Barthel ADL Index.;Muscle tone. Timepoint: Exactly before the treatment, in the sixth treatment session,and exactly after the treatment. Method of measurement: By using Modified Ashworth Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyyed Ali Javad Mousavi

Technology and Research Deputy of Iran University of Medical Sciences

research@iums.ac.ir+98 21 8670 2503

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026