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OpenTrials
Completed

NCT Number: NCT01869244

WOODCAST Hand Resting Splint - Study of User Experience

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

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Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Kuntoutus Orton Oy

Helsinki, 00280, Finland

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. User satisfaction

    Time frame: 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).

Sponsors and collaborators

Lead sponsor

Onbone Oy

Industry

Registry information

Official study title

User Experience From WOODCAST 2mm Hand Resting Splint

Important dates

Study start
2013
Primary completion
2016
Study completion
2016
First posted
Jun 5, 2013
Registry last updated
Jun 14, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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