Goal Attainment Scaling in Upper Limb Spasticity Treatment

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Rehabilitation Institute, Republic of Slovenia

About this trial

Patients after stroke with upper limb spasticity treated with botulinum toxin-A (BTX-A) will be included in this two-part study. In the first part, goal attainment scaling and comprehensive assessment of motor functioning will be performed before BTX-A application and after two weeks. In the second part, the patients will be randomised into a test group performing prescribed regular exercise for two weeks and a control group exercising at their own discretion during the same period, whereby the patients' health-related quality of life will be assessed at the beginning and end of the two-week period.

Eligibility criteria

Qualifiers

patient's or caregiver's approval

ischemic or hemorrhagic stroke diagnosed using head CT/MRI

at least one upper limb muscle spasticity (MAS ≥ 3)

candidate for BTX-A treatment or already given BTX-A in the past

Disqualifiers

aphasic patients without caregiver's presence

other neurological or musculoskeletal diseases that could affect the treatment outcome

Trial design

Treatments tested in this trial

  • Prescribed exercise program

Treatment groups

70 Participants
are divided into 2 treatment groups