Clinical trial Recruiting at 1 site Interventional Ages 45 to 65

Vojta therapy to improve posture and trunk control after stroke

Official title: Effects of Vojta Therapy on Posture and Trunk Control in Patients With Sub-acute Stroke

Run by University of Lahore · NCT07244952 · Data updated 2026-11-12

This study will see if adding Vojta reflex locomotion therapy to routine physical therapy helps adults with recent ischemic stroke improve posture, trunk control, and arm movement.

Quick facts

Study typeInterventional
Ages45 Years to 65 Years
SexAll
Enrollment62 (estimated)
SponsorUniversity of Lahore
Academic / other
Locations1 site (Lahore)
StatusRecruiting
StartedNovember 15, 2025
Main results expectedAugust 15, 2026
Study endsAugust 30, 2026
Registry record updatedNovember 28, 2025
Trial IDNCT07244952 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 45–65 with a first-time sub-acute ischemic stroke (7 days to 3 months), Brunnstrom stage 1–2, CT-confirmed ischemic stroke, arm muscle strength ≤2 on the MRC scale, NIHSS 16–20, premorbid modified Rankin ≤3, and who can achieve supported standing and sit for 30 seconds.

Probably not a fit

Patients with severe cognitive impairment, significant aphasia or communication limits, altered consciousness or dementia, postural hypotension, hemorrhagic stroke, or those outside the stated age/functional criteria are unlikely to benefit or be eligible.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The trial compares Vojta reflex locomotion therapy combined with routine physical therapy against routine physical therapy alone in adults with sub-acute ischemic stroke (7 days to 3 months post-stroke). Vojta therapy uses stimulation of specific reflex zones to trigger innate global movement patterns and engage postural muscles, while pose-estimation software records body angles and movement for objective analysis. Clinical measures of trunk control and upper-extremity motor function will be collected alongside the pose-estimation data to determine differences between groups. Participants meet defined motor and functional criteria and receive supervised in-person therapy sessions at the study site.

Why it matters

Potential benefit: If successful, adding Vojta therapy could improve postural stability, trunk control, and arm function after sub-acute ischemic stroke, potentially speeding functional recovery.

How similar studies have gone: Small studies and case reports have suggested potential benefits of Vojta therapy for postural control after neurological injury, but high-quality controlled evidence in stroke is limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 45-65 years
* Both males and females
* First time subacute stroke (7 days post stroke to 3 months)
* Brunnstrom stage 1,2
* A confirmed CT scan for subacute ischemic stroke
* A hemiplegia with score of ≤2 of medical research council scale for muscle strength of the arm (MRCS)
* Premorbid modified Rankin scale score ≤ 3
* Stroke patient who can achieve supported standing
* Patients having NIHSS score 16-20 will be included
* Patient who can achieve sitting for 30 seconds

Exclusion Criteria:

* Severe cognitive impairments that can hinder rehabilitation
* Limitations in communication due to aphasia
* Altered consciousness or dementia (Epple et al., 2020b)
* Patients suffering from postural hypotension

Where it's running

  • Dr Wajeeha Mahmood (PT)
    Lahore, Pakistan
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.