Acne scarring: protocol for development of a core outcome set for clinical trials

Introduction Acne scarring is one of the primary sequelae that affect patients with acne, with facial scarring occurring to some extent in 95% of patients with active acne. Subtypes include atrophic, hypertrophic and keloid scarring. Treatment options include topical and surgical approaches. Despite...

Full description

Saved in:
Bibliographic Details
Main Authors: Jamie J Kirkham, Murad Alam, Ian A Maher, Joseph F Sobanko, Todd V Cartee, Areeba Ahmed, Brian Cahn, Misha Haq, Eric Koza, Melissa S Ma, Victoria J Shi
Format: Article
Language:English
Published: BMJ Publishing Group 2025-04-01
Series:BMJ Open
Online Access:https://bmjopen.bmj.com/content/15/4/e088049.full
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850034592915914752
author Jamie J Kirkham
Murad Alam
Ian A Maher
Joseph F Sobanko
Todd V Cartee
Areeba Ahmed
Brian Cahn
Misha Haq
Eric Koza
Melissa S Ma
Victoria J Shi
author_facet Jamie J Kirkham
Murad Alam
Ian A Maher
Joseph F Sobanko
Todd V Cartee
Areeba Ahmed
Brian Cahn
Misha Haq
Eric Koza
Melissa S Ma
Victoria J Shi
author_sort Jamie J Kirkham
collection DOAJ
description Introduction Acne scarring is one of the primary sequelae that affect patients with acne, with facial scarring occurring to some extent in 95% of patients with active acne. Subtypes include atrophic, hypertrophic and keloid scarring. Treatment options include topical and surgical approaches. Despite numerous clinical trials focusing on acne scarring treatments, the absence of standardised outcome reporting across these trials raises concerns in evaluating treatment methods. To address this issue, this project aims to develop a core set of outcomes which should be uniformly assessed in all clinical trials involving acne scarring.Methods and analysis Outcomes will be extracted from four sources: a systematic literature review, patient interviews, printed and electronic sources and stakeholder involvement. The steering committee will assess the potential outcomes, adding or removing outcomes if needed. The Delphi process will be performed to understand the importance of outcomes. Two rounds of Delphi surveys will be completed by physicians, researchers and patients. Following this, a consensus meeting involving stakeholders will be held to refine the outcomes based on participant scores. The meeting will end in a voting process to determine a final recommended core outcome set (COS). This study will be conducted in collaboration with the Core Outcome Measures in Effectiveness Trials (COMET) initiative and the CHORD COUSIN Collaboration (C3). This study aims to develop a global COS to standardise assessment approaches in clinical trials of acne scarring. The final goal is to enhance uniformity of outcome reporting.Ethics and dissemination Ethical approval and consent to participate for the study have been granted by Northwestern University Institutional Review Board protocol ID: STU00097285. On completion of the COS, we plan to publish our results in peer-reviewed journals and send participants the finalised COS.PROSPERO registration details This study is registered with PROSPERO (CRD42023460964), COMET (754) and C3 (https://www.c3outcomes.org/improved-acne-scarring).
format Article
id doaj-art-02eee57db67e40fb9c0511bd5aa3bd2c
institution DOAJ
issn 2044-6055
language English
publishDate 2025-04-01
publisher BMJ Publishing Group
record_format Article
series BMJ Open
spelling doaj-art-02eee57db67e40fb9c0511bd5aa3bd2c2025-08-20T02:57:46ZengBMJ Publishing GroupBMJ Open2044-60552025-04-0115410.1136/bmjopen-2024-088049Acne scarring: protocol for development of a core outcome set for clinical trialsJamie J Kirkham0Murad Alam1Ian A Maher2Joseph F Sobanko3Todd V Cartee4Areeba Ahmed5Brian Cahn6Misha Haq7Eric Koza8Melissa S Ma9Victoria J Shi103 Centre for Biostatistics, The University of Manchester, Manchester, UK1 Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA4 Department of Dermatology, University of Minnesota, Minneapolis, Minnesota, USA5 Department of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA6 Penn State Health Milton S Hershey Medical Center, Hershey, Pennsylvania, USA1 Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA2 Department of Dermatology, University of Illinois Chicago, Chicago, Illinois, USA1 Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA1 Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA1 Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA1 Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USAIntroduction Acne scarring is one of the primary sequelae that affect patients with acne, with facial scarring occurring to some extent in 95% of patients with active acne. Subtypes include atrophic, hypertrophic and keloid scarring. Treatment options include topical and surgical approaches. Despite numerous clinical trials focusing on acne scarring treatments, the absence of standardised outcome reporting across these trials raises concerns in evaluating treatment methods. To address this issue, this project aims to develop a core set of outcomes which should be uniformly assessed in all clinical trials involving acne scarring.Methods and analysis Outcomes will be extracted from four sources: a systematic literature review, patient interviews, printed and electronic sources and stakeholder involvement. The steering committee will assess the potential outcomes, adding or removing outcomes if needed. The Delphi process will be performed to understand the importance of outcomes. Two rounds of Delphi surveys will be completed by physicians, researchers and patients. Following this, a consensus meeting involving stakeholders will be held to refine the outcomes based on participant scores. The meeting will end in a voting process to determine a final recommended core outcome set (COS). This study will be conducted in collaboration with the Core Outcome Measures in Effectiveness Trials (COMET) initiative and the CHORD COUSIN Collaboration (C3). This study aims to develop a global COS to standardise assessment approaches in clinical trials of acne scarring. The final goal is to enhance uniformity of outcome reporting.Ethics and dissemination Ethical approval and consent to participate for the study have been granted by Northwestern University Institutional Review Board protocol ID: STU00097285. On completion of the COS, we plan to publish our results in peer-reviewed journals and send participants the finalised COS.PROSPERO registration details This study is registered with PROSPERO (CRD42023460964), COMET (754) and C3 (https://www.c3outcomes.org/improved-acne-scarring).https://bmjopen.bmj.com/content/15/4/e088049.full
spellingShingle Jamie J Kirkham
Murad Alam
Ian A Maher
Joseph F Sobanko
Todd V Cartee
Areeba Ahmed
Brian Cahn
Misha Haq
Eric Koza
Melissa S Ma
Victoria J Shi
Acne scarring: protocol for development of a core outcome set for clinical trials
BMJ Open
title Acne scarring: protocol for development of a core outcome set for clinical trials
title_full Acne scarring: protocol for development of a core outcome set for clinical trials
title_fullStr Acne scarring: protocol for development of a core outcome set for clinical trials
title_full_unstemmed Acne scarring: protocol for development of a core outcome set for clinical trials
title_short Acne scarring: protocol for development of a core outcome set for clinical trials
title_sort acne scarring protocol for development of a core outcome set for clinical trials
url https://bmjopen.bmj.com/content/15/4/e088049.full
work_keys_str_mv AT jamiejkirkham acnescarringprotocolfordevelopmentofacoreoutcomesetforclinicaltrials
AT muradalam acnescarringprotocolfordevelopmentofacoreoutcomesetforclinicaltrials
AT ianamaher acnescarringprotocolfordevelopmentofacoreoutcomesetforclinicaltrials
AT josephfsobanko acnescarringprotocolfordevelopmentofacoreoutcomesetforclinicaltrials
AT toddvcartee acnescarringprotocolfordevelopmentofacoreoutcomesetforclinicaltrials
AT areebaahmed acnescarringprotocolfordevelopmentofacoreoutcomesetforclinicaltrials
AT briancahn acnescarringprotocolfordevelopmentofacoreoutcomesetforclinicaltrials
AT mishahaq acnescarringprotocolfordevelopmentofacoreoutcomesetforclinicaltrials
AT erickoza acnescarringprotocolfordevelopmentofacoreoutcomesetforclinicaltrials
AT melissasma acnescarringprotocolfordevelopmentofacoreoutcomesetforclinicaltrials
AT victoriajshi acnescarringprotocolfordevelopmentofacoreoutcomesetforclinicaltrials