Loading…

Pain

Select Protocol ID

Pain Catastrophizing Scale
#860201

Pain Catastrophizing Scale - Child Version (PCS-C)
#860202

Pain Catastrophizing Scale - Parent Version (PCS-P)
#860203

Coping Strategies Questionnaire
#860301

Pain Coping Questionnaire - Short Form
#860302

Patient-Reported Outcomes Measurement Information System (PROMIS®) Numeric Rating Scale v.1.0 - Pain Intensity - 1a
#860401

Faces Pain Scale-Revised (FPS-R)
#860402

Revised Face, Legs, Activity, Cry, Consolability (FLACC) Pain Tool
#860403

Patient-Reported Outcomes Measurement Information System (PROMIS®) Item Bank v1.1 - Pain Interference - Short Form 8a
#860501

Patient-Reported Outcomes Measurement Information System (PROMIS®) Pediatric Item Bank v2.0 - Pain Interference - Short Form 8a
#860502

Patient-Reported Outcome Measurement Information System (PROMIS®) Parent Proxy Item Bank v2.0 - Pain Interference - Short Form 8a
#860503

Childhood Arthritis and Rheumatology Research Alliance (CARRA) Pain Chart
#860602

Patient-Reported Outcomes Measurement Information System (PROMIS®) Pediatric Short Form v2.0 - Pain Quality - Affective 8a
#860701

Patient-Reported Outcomes Measurement Information System (PROMIS®) Scale v2.0 - Neuropathic Pain Quality 5a
#860704

Patient-Reported Outcomes Measurement Information System (PROMIS®) Scale v2.0 - Nociceptive Pain Quality 5a
#860703

Patient-Reported Outcomes Measurement Information System (PROMIS®) Pediatric Short Form v2.0 - Pain Quality - Sensory 8a
#860702

Patient Global Impression of Change (PGIC)
#860801

Patient-Reported Outcomes Measurement Information System® (PROMIS) Item Bank v2.1 - Mobility
#860901

Patient-Reported Outcomes Measurement Information System® (PROMIS) Pediatric Item Bank v2.0 - Mobility - Short Form 8a
#860902

Youth Acute Pain Functional Ability Questionnaire (YAPFAQ)
#860903

Sickle Cell Pain Diary
#860601

Sickle Cell Pain Burden Interview (SCPBI)
#860101
Release Date:

December 25, 2021

Scope of Collection
Element Considered Final Measures in Toolkit
Intensity Pain Intensity
Location Pain Location
Pain Quality Pain Quality Descriptors
Anxiety: Pain-related, state, trait, disorder
Catastrophizing Pain Catastrophizing
Coping Pain Coping
Emotional
Psychosocial
Self-efficacy
Social
Care utilization
Frequency
Pain Burden Pain Burden
Physical Interference/Impact Pain Interference
Physical Mobility
Medication use Treatment Response: Medication Use
Patient reported treatment, satisfaction, or effectiveness Patient Reported Impression of Change
Working Group Roster:

WG Members:

Amanda Brandow, DO, Co-Chair
Medical College of Wisconsin
Milwaukee, WI
Pat Carroll, MD, Co-Chair
Johns Hopkins University
Baltimore, MD
Nitya Bakshi, MD
Emory University School of Medicine
Atlanta, GA
Claudia Campbell, PhD
Johns Hopkins University
Baltimore, MD
Deepika Darbari, MD
Children's National Hospital
Washington, DC
Stephanie Guarino, MD
Nemours Children's Hospital
Wilmington, DE
Martha Kenney, MD
Duke University School of Medicine
Durham, NC
Wally Smith, MD
Virginia Commonwealth University
Richmond, VA
Jennifer Stinson, PhD, RN-EC, CPNP
The Hospital for Sick Children
Toronto, ON
William Zempsky, MD
Connecticut Children's Medical Center
Hartford, CT

Sickle Cell Disease Panel Liaison, WG Manager and WG Supervisor:

Mark Nelms, PhD, WG Supervisor
RTI International
Research Triangle Park, NC
David Williams, MEng, WG Manager
RTI International
Research Triangle Park, NC

Supplemental Information includes protocols that the Working Group or Expert Review Panel considered useful and highly relevant to the domain but do not meet the criteria for inclusion in the Toolkit.

Additional Information:

There is no additional information for this collection.

Measure Protocols Domain/Collection
Pain Catastrophizing Add to My Toolkit Pain Catastrophizing - Adult Sickle Cell Disease: Pain Specialty Collection
Add to My Toolkit Pain Catastrophizing - Child Sickle Cell Disease: Pain Specialty Collection
Add to My Toolkit Pain Catastrophizing - Parent Proxy Sickle Cell Disease: Pain Specialty Collection
Pain Coping Add to My Toolkit Pain Coping - Adult Sickle Cell Disease: Pain Specialty Collection
Add to My Toolkit Pain Coping - Child Sickle Cell Disease: Pain Specialty Collection
Pain Intensity Add to My Toolkit Pain Intensity - Adolescent and Adult Sickle Cell Disease: Pain Specialty Collection
Add to My Toolkit Pain Intensity - Child Sickle Cell Disease: Pain Specialty Collection
Add to My Toolkit Pain Intensity - Toddler Sickle Cell Disease: Pain Specialty Collection
Pain Interference Add to My Toolkit Pain Interference - Adult Sickle Cell Disease: Pain Specialty Collection
Add to My Toolkit Pain Interference - Child Sickle Cell Disease: Pain Specialty Collection
Add to My Toolkit Pain Interference - Parent Proxy Sickle Cell Disease: Pain Specialty Collection
Pain Location Add to My Toolkit Pain Location Body Map - Child Sickle Cell Disease: Pain Specialty Collection
Add to My Toolkit Sickle Cell Disease Pain Location Body Map - Adult Sickle Cell Disease: Pain Specialty Collection
Pain Quality Descriptors Add to My Toolkit Pain Quality Descriptors (Affective) - Children Sickle Cell Disease: Pain Specialty Collection
Add to My Toolkit Pain Quality Descriptors (Neuropathic) - Adult Sickle Cell Disease: Pain Specialty Collection
Add to My Toolkit Pain Quality Descriptors (Nociceptive) - Adult Sickle Cell Disease: Pain Specialty Collection
Add to My Toolkit Pain Quality Descriptors (Sensory) - Children Sickle Cell Disease: Pain Specialty Collection
Patient Reported Impression of Change Add to My Toolkit Patient Global Impression of Change Sickle Cell Disease: Pain Specialty Collection
Physical Mobility Add to My Toolkit Physical Mobility - Adult Sickle Cell Disease: Pain Specialty Collection
Add to My Toolkit Physical Mobility - Child Sickle Cell Disease: Pain Specialty Collection
Add to My Toolkit Physical Mobility - Hospitalized Individuals Sickle Cell Disease: Pain Specialty Collection
Pain Burden Add to My Toolkit Sickle Cell Pain Burden Interview Sickle Cell Disease: Pain Specialty Collection