WOODCAST Hand Resting Splint - Study of User Experience

User Experience From WOODCAST 2mm Hand Resting Splint

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01869244

Enrollment

Registered

2013-06-05

Start date

2013-04-30

Completion date

2016-09-30

Last updated

2017-06-14

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

Conditions

Patient Satisfaction

Brief summary

The aim of the study is to collect comments form users of new type of hand resting splint.

Detailed description

An ecologically friendly and biodegradable wood-plastic composite cast (WOODCAST) is used as a hand resting splint in this study.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 90 Years

Healthy volunteers

Inclusion criteria

* patient treatment involves hand resting splint; age of patient 18 - 90 years; skills with language Finnish language (written and spoken)

Exclusion criteria

* decreased co-operation of the patient; patient with multiple illnesses; malignancy; an illness affecting the general health.

Design outcomes

Primary

Measure	Time frame	Description
User satisfaction	2-4 weeks	After using hand resting splint for two weeks, patient will fill a questionaire. In the questionaire patient is asked to assess the used splint (e.g. functional performance, visual appearance), by giving points (from 1 to 10 points). Patient will use two splints from different materials during the treatment (both of the splint will be assessed by the patient).

Countries

Finland

Outcome results