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Completed

NCT Number: NCT02882971

Objective Pain Score for Chronic Pain Clinic Patients

Currently, there is no observational pain scale for use in the outpatient setting for adult patients. An observational pain scale can allow for objective measurement of pain in patients over time and after treatment without the bias associated with self-report. Currently chronic pain patients are asked to rate their pain many times throughout their care, often over years. This introduces a bias in reporting as a pain a person is currently experiencing will seem more severe then a remembered pain event. A behavioral pain scale would allow for an objective measurement of pain that is reliable across multiple raters and comparable over time, which can help in judging the success of pain treatments.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Milton S. Hershey Medical Center

Hershey, Pennsylvania, 17033, United States

About this study

This is a prospective observational study. No changes in therapy will be initiated due to the information gathered by its protocol. All medical decisions will be based on the management of the clinical team. Data will be gathered during the subject's clinical visit, from the subject, and from the nursing staff caring for the subject.

The Chronic Pain Behavioral Pain Scale for Adults was developed by the research team based on behavior pain scales used in other populations and the clinical expertise of Chronic Pain specialists in the Hershey Medical Center Chronic Pain department.

Patients will be scored on the Chronic Pain Behavioral Pain Scale for Adults and the standard 11 point numeric rating scale (Jensen, Turner et al., 1996), on intake. Scoring will be done by the patient's assigned nurse and a member of the research team, at the time when the numeric pain score is typically obtained. The patient will be scored again on both the Chronic Pain Behavioral Pain Scale for Adults and the standard numeric rating pain scale at the conclusion of their procedure, again at the time when the numerical pain score is typically obtained. Scoring will again be done by the patient's assigned nurse and a member of the research team. The Chronic Pain Behavioral Pain Scale for Adults will be tested for inter-rater reliability using the paired scores from the nurse and researcher for each subject. Concurrent Validity will be measured using comparison between the numeric rating scale and the behavioral pain scale on each subject at each time point. Construct validity will be measured by comparing the behavioral pain score before and after the interventional pain treatment.

For training purposes, the assigned nurse and research team member will be provided a copy of the "Chronic Pain Behavioral Pain Scale for Adults" chart to be utilized during their patient encounters. Each team member will be individually instructed in the use of the scale immediately preceding their first use of the scales. This training will include a discussion of the elements, the definition of behaviors, and the use of the scoring system.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults age 18-75
  • Patients able to self-report their pain using a validated pain scale
  • Patients of the chronic pain clinic who will be receiving a pain treatment procedure
  • English speaking
  • Received and signed a consent to participate in the study

Exclusion criteria

  • Pregnant and lactating women
  • Patient with chronic malignant pain
  • Patients less than 18
  • Patient older than 75
  • Patients with dementia
  • Non-English speaking patients
  • Patients unable to do a self-report pain scale
  • Uncontrolled psychiatric conditions
  • Uncontrolled substance abuse issues
  • Patient's lost to follow-up
  • Patients who don't wish to participate

Treatment and study plan

Pain assessment

Behavioral

To create an objective observational pain scoring system and validate.

Primary outcomes

  1. Patient's pre-procedure pain score using the Chronic Pain Behavioral Scale for Adults.

    Time frame: Within 30 minutes prior to intervention designed to alleviate pain

    2 observers will use the new Chronic Pain Behavioral Scale for Adults to measure the patient's pain before a procedure to alleviate pain.

  2. Patient's pre-procedure pain score using the standard 11-point numerical rating scale.

    Time frame: Within 30 minutes prior to an intervention designed to alleviate pain

    The patient will be asked to rate their pain, using the standard 11-point numerical rating scale, before a procedure to alleviate pain.

Secondary outcomes

  1. Patient's post-procedure pain score using the Chronic Pain Behavioral Scale for Adults.

    Time frame: Within 3 h after an intervention designed to alleviate pain

    2 observers will use the new Chronic Pain Behavioral Scale for Adults to measure the patient's pain before a procedure to alleviate pain.

  2. Patient's post-procedure pain score using the standard 11-point numerical rating scale.

    Time frame: Within 3 h after an intervention designed to alleviate pain

    The patient will be asked to rate their pain, using the standard 11-point numerical rating scale, before a procedure to alleviate pain.

Sponsors and collaborators

Lead sponsor

Milton S. Hershey Medical Center

Other

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Aug 30, 2016
Registry last updated
Feb 7, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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