WOODCAST Hand Resting Splint - Study of User Experience

User Experience From WOODCAST 2mm Hand Resting Splint

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

Study Overview

• Status: Completed
• Conditions: Patient Satisfaction

Detailed Description

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

• Study Type: Observational
• Enrollment (Actual): 18

Contacts and Locations

Study Locations

• Finland
  • Helsinki, Finland, 00280
    • Kuntoutus Orton Oy

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 90 years (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Non-Probability Sample

Study Population

Patients whos treatment involves a hand resting splint. Finnish language skills (written and spoken).

Description

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.

Study Plan

How is the study designed?

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort
hand resting splint; Patients with hand resting splint treatment

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
User satisfaction	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).	2-4 weeks

Collaborators and Investigators

• Sponsor: Onbone Oy
• Investigators: Principal Investigator: Nina Lindfors, PhD, MD, Helsinki University Central Hospital

Study record dates

Study Major Dates

• Study Start: April 1, 2013
• Primary Completion (ACTUAL): September 1, 2016
• Study Completion (ACTUAL): September 1, 2016

Study Registration Dates

• First Submitted: May 31, 2013
• First Submitted That Met QC Criteria: June 4, 2013
• First Posted (ESTIMATE): June 5, 2013

Study Record Updates

• Last Update Posted (ACTUAL): June 14, 2017
• Last Update Submitted That Met QC Criteria: June 13, 2017
• Last Verified: June 1, 2017

More Information

Terms related to this study

• Other Study ID Numbers: 152/13/03/02/2013

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO