Results From a Health System-wide Implementation of a Quality of Life Questionnaire

Study summary

The purpose of this retrospective chart review pilot study is to research the results and scores of the QOL questionnaire implemented across Allina Health clinics. This study will investigate average QOL scores by clinical population and demographic group, the change in scores over time, and the effect of clinical interventions on QOL scores. The results will provide insight into QOL trends within different patient populations and provide guidance regarding optimal treatment plans so that Allina caregivers can positively impact patients' QOL.

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Key things to know

Main goalNot specified

This describes the study’s primary purpose.

What is being studiedPROMIS-10 questionnaire

The study team can explain what participation involves.

Who it may be forMedical Oncology · Cardiology

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Jan 11, 2017 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Observational

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?Allina Health System

Study sponsor

Study overview

What this study is about

Purpose: Not specified
Study type: Observational
Phase: Not applicable
Sponsor: Allina Health System
Interventions being studied: Other: PROMIS-10 questionnaire

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How this study is categorized

These labels come from structured fields and exact terms in the public record.

Study topics

Survivorship and quality of life→

Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria

patients seen at an Allina Health outpatient facility who complete a PROMIS-10 questionnaire between July 1, 2012 and December 31, 2016.

Reasons someone may not be able to joinExclusion criteria

patients who did not allow their records to be used for research purposes are not included in the study

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

Study sites

U.S. locations

Abbott Northwestern HospitalMinneapolis, Minnesota

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jan 11, 2017. Always confirm current availability with the study team.

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