Pilot Evaluation to Assess the Clinical and Economic Impact of Pfizer's Pain Management Program (painPREMIER) in the Treatment of Low Back Pain, in an Occupational Health Care Setting in Finland

NCT ID: NCT01787565

Last Updated: 2016-04-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Total Enrollment

86 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-01-31

Study Completion Date

2014-01-31

Brief Summary

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The aim of this investigation is to determine whether the use of painPREMIER will significantly improve function in patients with low back pain in an occupational health clinical setting. painPREMIER is a tool that assists clinicians in the accurate diagnosis of back pain and associated problems in order to treat them most effectively.

Detailed Description

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Patients presenting at feeder sites to be referred to low back pain clinic and assessed for eligibility A decision was made to terminate this study on 09 OCT 2013. The study was terminated for operational/business reasons. This study was not terminated for reasons of safety or efficacy.

Conditions

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Back Pain

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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painPREMIER cohort

painPREMIER cohort

Intervention Type OTHER

Low back pain patients prospectively recruited during the study period and managed with painPREMIER.

Control cohort

Control cohort

Intervention Type OTHER

A matched group of low back pain patients not managed with painPREMIER.

Interventions

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painPREMIER cohort

Low back pain patients prospectively recruited during the study period and managed with painPREMIER.

Intervention Type OTHER

Control cohort

A matched group of low back pain patients not managed with painPREMIER.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* New episode of low back pain
* Member of Terveystalo health insurance scheme

Exclusion Criteria

* Previous back pain related healthcare visit in the last 3 months
* Patients identified as having a 'red flag' condition
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Terveystalo

OTHER

Sponsor Role collaborator

Pfizer

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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Pfizer Investigational Site

Helsinki, , Finland

Site Status

Countries

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Finland

Related Links

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https://trialinfoemail.pfizer.com/pages/landing.aspx?StudyID=X9001016

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Other Identifiers

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X9001016

Identifier Type: -

Identifier Source: org_study_id

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