Fact CheckerSign in

NCT07616622Enrolling by invitation

Roods vs PNF for Upper Limb Function in Acute MCA Stroke

Comparison Between Roods Facilitatory Techniques and Sequential PNF Pattern on Upper Limb Function in Acute Phase of Middle Cerebral Artery Stroke Patients

Source: ClinicalTrials.gov · Last updated 1 Jun 2026

Brief summary (registry, in English)

Middle cerebral artery (MCA) stroke often causes weakness or stiffness in the arm and hand, making daily activities difficult. This study compares two physical therapy approaches - Rood's facilitatory techniques (using touch, quick stretch, and ice to activate muscles) and PNF sequential patterns (using diagonal movement patterns) - to improve arm function in acute stroke patients. Both groups will also receive neuromuscular electrical stimulation (NMES). A total of 28 patients will be randomly assigned to one of two groups and receive treatment three times per week for eight weeks. Arm function will be measured using the Fugl-Meyer Assessment, and muscle stiffness will be measured using the Modified Ashworth Scale before and after treatment.

Status (registry)
Enrolling by invitation
Study type
Interventional
Enrollment
28 (estimated)
First submitted
23 May 2026
Start date
1 Jan 2026
Primary completion date
15 Jun 2026
Lead sponsor
University of Faisalabad
Diseases
Stroke
NCT number
NCT07616622

What you commit to

  • Study type: Interventional
  • Planned participants: 28
  • From 1 Jan 2026 to the primary completion date, 15 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Severe coexisting medical disorders (heart, liver, kidney failure; malignant tumors)
  • Severe cognitive impairment or aphasia preventing adherence or consent (MMSE below threshold)
  • Skin sores, ulcers, or hypersensitivity (e.g., to cold) contraindicated for sensory stimulation

Other

  • Fixed musculoskeletal abnormalities or contracture in affected upper limb
  • Refusal or inability to give informed consent

Who the study is looking for

  • Adults (40-60 years) with confirmed MCA stroke (ischemic or hemorrhagic) on neuroimaging (CT or MRI)
  • Mild to moderate upper limb motor dysfunction with MRC ≥2 for proximal limb motor strength
  • Cognitive competence to understand instructions (MoCA ≥19 or equivalent)
  • First stroke, acute or subacute phase
  • Willingness to provide written informed consent
  • Both male and female genders

Age in the registry: 40 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The University of Faisalabad
Coordinator of this site? Confirm its status
FaisalābadPakistanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.