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Development of the pediatric daily ulcerative colitis signs and symptoms scale (DUCS): qualitative research findings
Emuella Flood1, Debra G Silberg2, Beverly Romero3
1ICON plc, 820 W Diamond Ave, Ste 100, Gaithersburg, MD, 20878, USA. emuella.flood@iconplc.com.
Insights
A new Daily Ulcerative Colitis Signs and Symptoms Scale (DUCS) was developed for children with mild to moderate ulcerative colitis (UC). This patient-reported outcome measure effectively captures key daily UC symptoms in pediatric clinical trials.
Area of Science:
- Pediatric Gastroenterology
- Clinical Trial Methodology
- Patient-Reported Outcome Measures
Background:
- Ulcerative colitis (UC) significantly impacts children's quality of life.
- Existing outcome measures may not fully capture the daily experiences of pediatric UC patients.
- Development of reliable instruments is crucial for assessing treatment efficacy in pediatric UC.
Purpose of the Study:
- To develop patient-reported (PRO) and observer-reported (ObsRO) outcome measures for ulcerative colitis (UC) signs and symptoms in children aged 5-17 with mild to moderate UC.
- To create the Daily Ulcerative Colitis Signs and Symptoms Scale (DUCS) suitable for use in clinical trials.
Main Methods:
- Two-phase development process: Phase I (concept elicitation, item generation) and Phase II (cognitive debriefing, usability/feasibility assessment).
- Recruitment across five US clinical sites, a research agency, and online advertising.
- Thematic and content analysis of interviews, iterative analysis of debriefing, and US Food and Drug Administration (FDA) feedback incorporated.
Main Results:
- A core set of seven key signs and symptoms identified: abdominal pain, blood in stool, frequent stools, diarrhea, stool urgency, nighttime stools, and tiredness.
- Participant and FDA feedback led to refined item wording, graphics, response scales, and inclusion of nighttime symptoms.
- The DUCS scale demonstrated usability and feasibility in pediatric UC patients.
Conclusions:
- The developed Daily Ulcerative Colitis Signs and Symptoms Scale (DUCS) PRO and ObsRO eDiaries are content-valid instruments.
- DUCS effectively captures daily signs and symptoms of pediatric UC in a clinical trial setting.
- This tool supports better assessment and management of mild to moderate UC in children.
Background:
The purpose of this study is to develop patient-reported (PRO) and observer-reported (ObsRO) outcome measures of ulcerative colitis (UC) signs/symptoms in children aged 5-17 with mild/moderate UC. The daily ulcerative colitis signs and symptoms scale (DUCS) was developed in two phases. Phase I involved concept elicitation interviews with patients and healthcare providers, review of website posts and item generation. Phase II involved cognitive debriefing and assessment of usability and feasibility of the eDiaries. Participants were recruited from five US clinical sites, a research recruitment agency, and internet advertising. Thematic and content analysis was performed to identify concepts from Phase I. The Phase II cognitive debriefing interviews were analyzed iteratively to identify problems with clarity and relevance of eDiary content. The US Food and Drug Administration (FDA) also reviewed and provided feedback on the eDiaries.
Results:
Phase I included 32 participants (22 remission; 10 active disease). Phase II included 38 participants (22 remission; 16 active disease). A core set of seven signs and symptoms emerged that were reported by at least 30% of the patients interviewed: abdominal pain, blood in stool, frequent stools, diarrhea, stool urgency, nighttime stools, and tiredness. Participant input influenced changes such as refinement of item wording, revision of graphics, and selection of response scales. Revisions suggested by FDA included simplifying the response scale and adding questions to capture symptoms during sleeping hours.
Conclusions:
The findings of instrument development suggest that the DUCS PRO and ObsRO eDiaries are content-valid instruments for capturing the daily signs and symptoms of pediatric patients with mild to moderate UC in a clinical trial setting.
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