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Protocol - Pain Interference - Child

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Description

The Patient-Reported Outcomes Measurement Information System (PROMIS®) Pediatric Item Bank v2.0 - Pain Interference - Short Form 8a is an 8-item self-report questionnaire completed by children that assesses how pain impacts a childs daily activities of living and the enjoyment of those activities. This protocol was validated in individuals aged 8- to 17-years-old.

Specific Instructions

The Sickle Cell Disease Pain Working Group recommends the use of the Pain Interference – Parent-proxy protocol for children under the age of 8-years-old.

The PhenX Working Group recommends this PROMIS® protocol. For additional information regarding PROMIS® instruments (including scoring, validity, and interpretation) please visit: www.healthmeasures.net. For specific information about this instrument, please visit: www.healthmeasures.net/index.php?option=com_instruments&view=measure&id=711&Itemid=992

Protocol

PROMIS® Pediatric Item Bank v2.0 - Pain Interference - Short Form 8a


In the past 7 days….


1. I felt angry when I had pain.

1 [ ] Never

2 [ ] Almost Never

3 [ ] Sometimes

4 [ ] Often

5 [ ] Almost Always


2. I had trouble doing schoolwork when I had pain.

1 [ ] Never

2 [ ] Almost Never

3 [ ] Sometimes

4 [ ] Often

5 [ ] Almost Always


3. I had trouble sleeping when I had pain.

1 [ ] Never

2 [ ] Almost Never

3 [ ] Sometimes

4 [ ] Often

5 [ ] Almost Always


4. It was hard for me to pay attention when I had pain.

1 [ ] Never

2 [ ] Almost Never

3 [ ] Sometimes

4 [ ] Often

5 [ ] Almost Always


5. It was hard for me to run when I had pain.

1 [ ] Never

2 [ ] Almost Never

3 [ ] Sometimes

4 [ ] Often

5 [ ] Almost Always


6. It was hard for me to walk one block when I had pain.

1 [ ] Never

2 [ ] Almost Never

3 [ ] Sometimes

4 [ ] Often

5 [ ] Almost Always


7. It was hard to have fun when I had pain.

1 [ ] Never

2 [ ] Almost Never

3 [ ] Sometimes

4 [ ] Often

5 [ ] Almost Always


8. It was hard to stay standing when I had pain.

1 [ ] Never

2 [ ] Almost Never

3 [ ] Sometimes

4 [ ] Often

5 [ ] Almost Always

Availability

Available

Personnel and Training Required

None

Equipment Needs

None

Requirements
Requirement CategoryRequired
Major equipment No
Specialized training No
Specialized requirements for biospecimen collection No
Average time of greater than 15 minutes in an unaffected individual No
Mode of Administration

Self-administered questionnaire

Lifestage

Child, Adolescent

Participants

Children and Adolescents aged 8- to 17-years-old

Selection Rationale

This Patient-Reported Outcomes Measurement Information System (PROMIS®) measure is psychometrically robust and has been verified in patients with sickle cell disease. The availability of both pediatric and adult measures allows for comparison across the lifespan. Additionally, having both self and parent/proxy reports available is important for use with the pediatric population.

Language

Dutch, English, French, German, Hungarian, Icelandic, Italian, Japanese, Mandarin Chinese, Portuguese, Spanish, Traditional Chinese, Turkish

Standards
StandardNameIDSource
caDSR Common Data Elements (CDE) Pain Interference-Child Assessment Score   7997204 CDE Browser
Derived Variables

None

Process and Review

Not Applicable

Protocol Name from Source

Patient-Reported Outcomes Measurement Information System (PROMIS®) Pediatric Item Bank v2.0 - Pain Interference - Short Form 8a

Source

Quinn, H., Thissen, D., Liu, Y., Magnus, B., Lai, J. S., Amtmann, D., Varni, J. W., Gross, H. E., & DeWalt, D. A. (2014). Using item response theory to enrich and expand the PROMIS® pediatric self report banks. Health and Quality of Life Outcomes, 12, 160.

General References

Dampier, C., Barry, V., Gross, H. E., Lui, Y., Thornburg, C. D., DeWalt, D. A., & Reeve, B. B. (2016). Initial evaluation of the pediatric PROMIS® health domains in children and adolescents with sickle cell disease. Pediatric Blood & Cancer, 63(6), 1031-1037.

Singh, A., & Panepinto, J. A. (2019). Clinical meaning of PROMIS pain domains for children with sickle cell disease. Blood Advances, 3(15), 2244-2249.

Amtmann, D., Cook, K. F., Jensen, M. P., Chen, W. H., Choi, S., Revicki, D., ... Lai, J-S. (2010). Development of a PROMIS item bank to measure pain interference. Pain, 150(1), 173-182.

Protocol ID

860502

Variables
Export Variables
Variable Name Variable IDVariable DescriptiondbGaP Mapping
Pain
Measure Name

Pain Interference

Release Date

May 18, 2022

Definition

The extent to which the experience of pain interferes with a person's daily life. 

Purpose

Pain is a complex multidimensional experience that extends beyond its presence and severity. The presence of pain can have an impact on an individual's quality of life including interfering with activities at home, socially, and in the general enjoyment of life. This measure provides a comprehensive assessment of how a person's pain is interfering across different factors.

Keywords

Pain, sickle cell disease, Patient-Reported Outcomes Measurement Information System, PROMIS®, National Institutes of Health, NIH

Measure Protocols
Protocol ID Protocol Name
860501 Pain Interference - Adult
860502 Pain Interference - Child
860503 Pain Interference - Parent Proxy
Publications

There are no publications listed for this protocol.