NCT01869244

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
18

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Apr 2013

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2013

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

May 31, 2013

Completed
5 days until next milestone

First Posted

Study publicly available on registry

June 5, 2013

Completed
3.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2016

Completed
Last Updated

June 14, 2017

Status Verified

June 1, 2017

Enrollment Period

3.4 years

First QC Date

May 31, 2013

Last Update Submit

June 13, 2017

Conditions

Patient Satisfaction

Outcome Measures

Primary Outcomes (1)

  • 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

Study Arms (1)

hand resting splint

Patients with hand resting splint treatment

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kuntoutus Orton Oy

Helsinki, 00280, Finland

Location

Related Links

MeSH Terms

Conditions

Patient Satisfaction

Condition Hierarchy (Ancestors)

Treatment Adherence and ComplianceHealth BehaviorBehavior

Study Officials

  • Nina Lindfors, PhD, MD

    Helsinki University Central Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 31, 2013

First Posted

June 5, 2013

Study Start

April 1, 2013

Primary Completion

September 1, 2016

Study Completion

September 1, 2016

Last Updated

June 14, 2017

Record last verified: 2017-06

Data Sharing

IPD Sharing
Will not share

Locations

FI(1)