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Optimizing Chronic Pain Management Through Patient Engagement With Quality of Life Measures (OPTIQUAL)

U

University of North Texas Health Science Center

Status

Completed

Conditions

Chronic Low Back Pain

Treatments

Other: Health-Related Quality of Life Report

Study type

Interventional

Funder types

Other

Identifiers

NCT04168437
2015-169

Details and patient eligibility

About

This study evaluates the use of a health-related quality of life report based on the SPADE cluster (sleep disturbance, pain interference with activities, anxiety, depression, and low energy/fatigue) derived from the PROMIS-29 instrument in patients with chronic low back pain. Half of the participants will receive the report, while the other half will not.

Full description

The health-related quality of life report provides participants with an overall score on the SPADE cluster and scores on each of its five component scales. The recently released Federal Pain Research Strategy states that pain cannot be measured in isolation, but rather should be assessed in conjunction with other outcome measures in 'non-pain domains,' such as quality of life. It recognizes that pain may be affected by, and affect, such patient attributes as sleep, mood, cognition, function, and quality of life. Further, the report states that improvement in pain without concomitant improvement in other domains may not constitute a clinically meaningful outcome. This study primarily aims to assess the utility of a health-related quality of life report in improving quality of life, back pain intensity, and back-related disability in participants with chronic low back pain. Another aspect of the study will be to determine how the health-related quality of life report may impact the physician-patient interaction. This will be assessed using validated measures of physician interpersonal manner, empathy, and communication style, as well as end-of-trial survey data acquired from participants assigned to the experimental group. The survey will include an overall assessment of the report, as well as specific actions attributed to the report.

Enrollment

331 patients

Sex

All

Ages

21 to 79 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Chronic Low Back Pain AND SPADE Cluster Score ≥ 55

Exclusion criteria

  • Absence of Chronic Low Back Pain OR SPADE Cluster Score < 55

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

331 participants in 2 patient groups

Health-Related Quality of Life Report
Experimental group
Description:
Participants randomized to this arm will receive the 2- page Health-Related Quality of Life Report.
Treatment:
Other: Health-Related Quality of Life Report
Wait List to Receive the Report
No Intervention group
Description:
Participants randomized to this arm will receive the 2- page Health-Related Quality of Life Report following completion of the study.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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