NCT02256202

Brief Summary

There are actually no standardized quality assurance procedures included in pain treatment processes. In this observational, feasibility study the use of tablet-Personal Computer (PC) is tested in pain therapy centres using the validated questionnaire "Activity Index". The acceptance of electronic data capturing is tested in patients and therapy teams (doctors and nurses).

Trial Health

87
On Track

Trial Health Score

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

Enrollment
64

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Aug 2014

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

August 1, 2014

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

September 25, 2014

Completed
8 days until next milestone

First Posted

Study publicly available on registry

October 3, 2014

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2015

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2015

Completed
Last Updated

October 23, 2015

Status Verified

October 1, 2015

Enrollment Period

7 months

First QC Date

September 25, 2014

Last Update Submit

October 22, 2015

Conditions

Pain

Outcome Measures

Primary Outcomes (1)

  • Feasibility of Tablet-PC in interviewing pain patients

    The feasibility of the Tablet-PC in EDC will be assessed by standardized interviews (three times) of the study doctor, the study nurse and the patient.

    6-12 months

Secondary Outcomes (1)

  • Problems in application of EDC in Tablet-PC

    12 months

Interventions

InterviewOTHER

Monitoring interviews to show medical and economic advantages of given therapy

Eligibility Criteria

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

Back pain patients

You may qualify if:

  • Willingness for therapeutic pain injection in lumbar spine

You may not qualify if:

  • Cognitive impairment, technical Problems in interviewing patients

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Stadtspital Triemli

Zurich, Canton of Zurich, 8063, Switzerland

Location

MeSH Terms

Conditions

Pain

Interventions

Interviews as Topic

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Robert Theiler

    Stadtspital Triemli Zurich, Department of Rheumatology

    PRINCIPAL INVESTIGATOR

Study Design

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

Study Record Dates

First Submitted

September 25, 2014

First Posted

October 3, 2014

Study Start

August 1, 2014

Primary Completion

March 1, 2015

Study Completion

October 1, 2015

Last Updated

October 23, 2015

Record last verified: 2015-10

Locations

CH(1)