Does adaptation of prism glasses affect the pusher symptoms

Does adaptation of prism glasses affect the pusher symptoms - BPAPS

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00029201

Enrollment

Registered

2022-06-07

Start date

2021-11-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

R29.3 R29.5

Interventions

Group 1: Intervention: continuous prism adaptation. First, the weight distribution value is recorded without prism glasses. The glasses are put on for the duration of the intervention (80x tapping g

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Minimum age of 18 years -Pusher symptoms after right hemisphere lesion. The cut-off value when measuring with the "Tymo" sensor plate from the Tyromotion brand is 50. The values ??are recorded simultaneously on both the right and left side of the body by sitting on the "Tymo" sensor plate and are given as a percentage. If the value is 50, there is an increased weight shift on the side. -Sufficient resilience for at least 30 minutes -Regular ability to mobilize at least 80 % of the planned therapies

Exclusion criteria

Exclusion criteria: - dementia - Therapeutic mobilization ability for less than 80% of scheduled therapy sessions

Design outcomes

Primary

Measure	Time frame
Aim: to treat a total of 30 'pusher' patients with prism adaptation therapy. The measurements of the weight distribution on the sensor plate `Tymo` take place at seven measuring points: T1 = Day 1 of recruitment (for baseline survey) T2 = 3 days later (for baseline survey) T3 = another 3 days later (for baseline survey) T4 = before completing the first intervention (day 10) T4.1 = Immediately following the first intervention T5 = before completing the second intervention (day 13) T5.1 = immediately following the second intervention T6 = before completing the third intervention (day 16) T6.1 = immediately following the third intervention T7 = 14 days after completing the third intervention (day 30) (baseline baseline measurement) The following measurement instruments will be used (at the beginning and end of the study): - Clinical Scale for Contraversive Pusher Symptoms (CPS) - Degrees of strength according to Janda	—

Measure

Time frame

Aim: to treat a total of 30 'pusher' patients with prism adaptation therapy. The measurements of the weight distribution on the sensor plate `Tymo` take place at seven measuring points: T1 = Day 1 of recruitment (for baseline survey) T2 = 3 days later (for baseline survey) T3 = another 3 days later (for baseline survey) T4 = before completing the first intervention (day 10) T4.1 = Immediately following the first intervention T5 = before completing the second intervention (day 13) T5.1 = immediately following the second intervention T6 = before completing the third intervention (day 16) T6.1 = immediately following the third intervention T7 = 14 days after completing the third intervention (day 30) (baseline baseline measurement) The following measurement instruments will be used (at the beginning and end of the study): - Clinical Scale for Contraversive Pusher Symptoms (CPS) - Degrees of strength according to Janda

—

Secondary

Measure	Time frame
The following measuring instruments are collected in a blinded manner: - Early Rehabilitation Barthel Index - Functional Independence Measure	—

Countries

Germany

Contacts

Public ContactAnna Elisabeth Pape

Therapie Somatik, Klinikum Bremen-Ost

AnnaElisabeth.Pape@klinikum-bremen-ost.de004042140862663

Outcome results

None listed

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