Mode
Text Size
Log in / Sign up
N/A Completed N=53

Feasibility of Measuring Vertical Perception in Acute Stroke

Source: ClinicalTrials.gov NCT06301815 ↗
Enrolled (actual)
53
Serious AEs
0.0%
Results posted
Jun 2025
Primary outcomePrimary: Bucket Test to Measure Subjective Visual Vertical (SVV). — 3.2 Degrees

Summary

The goal of this observational study is to establish if it is feasible to identify vertical perception deficits in people with acute stroke. The primary purpose to the study is: • To establish the feasibility of completing the Catherine Bergego Scale, Scale for Contraversive Pushing (SCP) and bucket test in a clinical environment with acute stroke patients to assist with identification of vertical perception loss. Participants will be asked to complete the assessments with a therapist 48 hours after admission. If they are not completed for any reason attempts will be made to complete them at one, two and four weeks after admission. Some participants will have them completed again on discharge. The Catherine Bergego Scale and SCP are observational and will involve a therapist watching the participant undertake daily activities. The bucket test involves a therapist placing a bucket in front of the face of the participant and asking them to identify when a line on the bottom of the bucket is vertical. Acceptabiliy and feasibility will be further investigated using a survey of participants who complete the assessments and through focus groups with the rehabilitation professionals admininstering the assessments. If it is feasible and acceptable to complete these assessments then further research can use them as an acceptable measure of vertical alignment in the clinical setting.

Outcome Measures

OutcomeResultp-value
PRIMARY
Bucket Test to Measure Subjective Visual Vertical (SVV).
3.2
PRIMARY
Catherine Bergego Scale to Measure Neglect.
PRIMARY
Scale for Contraversive Pushing to Measure Lateropulsion

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of first stroke by stroke consultant based on clinical or radiographical findings
  • Admitted to stroke unit with a length of stay of over 72 hours
  • Ability to consent or an advocate to consent on their behalf
  • Pre-morbid Modified Rankin Scale of less than 4

Exclusion Criteria

  • Under the age of 18
  • Diagnosis of Transient Ischaemic Attack (TIA)
  • Previous diagnosis of stroke or other neurological diagnosis affecting the brain with residual impairment
  • Patients on an end of life pathway
  • Patients with pre-morbid visual impairment that will not allow them to see the bucket test. Glasses can be worn.
  • Inability to speak the English language and no interpreter can be found
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT06301815). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

Back to search