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Sensory Referral in Stroke - a mixed methods feasibility study

Sensory Referral in Stroke - a mixed methods feasibility study

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
DRKS
Registry ID
DRKS00018991
Enrollment
15
Registered
2019-11-19
Start date
2019-11-19
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

I63 I61

Interventions

Group 1: A rubber replacement and, if preferred, the participants unaffected hand or foot will be stimulated with paint brushes and the researcher's hand. This will be watched by the participant in a

Sponsors

University of Leicester
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: • Willing and able to give informed consent for participation in the study; • Aged 18 years or above; • Has had a physician-confirmed stroke at least 6 months ago and is suffering from unilateral numbness since having had a stroke; • Able to communicate with the researchers • Able (in the Investigators’ opinion) and willing to comply with all local and procedural study requirements.

Exclusion criteria

Exclusion criteria: • Unwillingness or inability to consent; • Presence of sensory impairment from origin other than stroke or itchy skin; • Additional severe neurological diseases or any symptoms of tremor; • Constant pain or pain on touch or pressure in hands or feet; • Inability to maintain a stable (supported) position of the hand on the table; • A position that would be painful if sensation was restored; • Inability to focus attention for 10 minutes; • Acute major events in the past month; • Any visual impairment that excludes clear vision of their own foot and hand; • Any psychosomatic or psychiatric diseases (including drug addictions), where sensory stimulation may cause anxiety or disappointment in case of no-improvement; • Ladies who are pregnant or lactating; • Any significant disease or disorder which, after consulting the medical supervisors of the research team, may either put the participants at risk because of participation in the study, or may influence the result of the study, or the participant’s ability to participate in the study.

Design outcomes

Primary

MeasureTime frame
Feasibility Study: 1. What recruitment strategies and rates are feasible for including people with stroke from various settings? 2. Are the proposed interventions and outcome measures acceptable for people with stroke, and what experiences and attitudes do they have?

Secondary

MeasureTime frame
Fugl-Meyer Assessment, Box and Block Test, Berg Balance Scale, Goal Attainment Scale, EuroQol-5D, and a sensation map; questions regarding acceptability and tolerability of assessments and intervention, and regarding quality of the perception with rating of the strength using NRS; Time points: first, forth and follow-up session.

Countries

Germany, United Kingdom

Contacts

Public ContactAnnegret Hagenberg

University of Leicester

ah413@le.ac.uk+44 116 229 7605

Outcome results

None listed

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