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A Core set of patient‐reported outcome measures to measure quality of life in obesity treatment research

  • Phillip J. Dijkhorst
  • , Claire E. E. de Vries
  • , Caroline B. Terwee
  • , Ignace M. C. Janssen
  • , Ronald S. L. Liem
  • , Bart A. van Wagensveld
  • , Johan Ottosson
  • , Bruno Halpern
  • , Stuart W. Flint
  • , Elisabeth F.C. van Rossum
  • , Alend Saadi
  • , Lisa West-Smith
  • , Mary O’Kane
  • , Jason C.G. Halford
  • , Karen D. Coulman
  • , Salman Al-Sabah
  • , John B. Dixon
  • , Wendy A. Brown
  • , Ximena Ramos Salas
  • , Maarten M. Hoogbergen
  • Sally Abbott, Alyssa J. Budin, Jennifer F. Holland, Lotte Poulsen, Richard Welbourn, Bernardo Rea Ruanova, John M. Morton, Francois Pattou, Erman O. Akpinar, Stephanie Sogg, Jacques M. Himpens, Vanessa Osborne, Natasja Wijling, Laura Divine, Nadya Isack, Susie Birney, J. M. Bernadette Keenan, Joe Nadglowski, Jacqueline Bowman, Ken Clare, Riccardo Meloni, Sandra de Blaeij, Theodore K. Kyle, Melanie Bahlke, Andrew Healing, Ian Patton, Valerie M. Monpellier
    • OLVG
    • VU University Amsterdam
    • Nederlandse Obesitas Kliniek
    • Erasmus University Medical Center
    • Neuchâtel Hospital
    • University of Lausanne
    • University of Cincinnati College of Medicine
    • Leeds Teaching Hospitals NHS Trust
    • University of Leeds
    • Kuwait University
    • Swinburne University of Technology
    • Monash University
    • Obesity Canada
    • European Association for the Study of Obesity
    • University of Southern Denmark
    • Musgrove Park Hospital
    • Dutch Association for Overweight and Obesity
    • People Living With Obesity Representative
    • Obesity Empowerment Network
    • European Coalition for People Living With Obesity
    • The Belgian Foundation for the Rights of People living with obesity
    • Obesity Action Coalition
    • Adipositascirurgie Selbsthilfe Deutschland E.V.
    • Groene Hart Ziekenhuis
    • NMC Royal Hospital
    • Örebro University
    • Hospital Nove de Julho
    • Brazilian Association for the Study of Obesity
    • NIHR Bristol Biomedical Research Centre
    • University of Bristol
    • Catharina Ziekenhuis
    • University Hospitals Coventry and Warwickshire NHS Trust
    • Odense University Hospital
    • Lontoft, Nyhoj and Poulsen Plastic Surgery
    • Yale School of Medicine
    • Centre Hospitalier Universitaire de Lille
    • University of Lille
    • Maastricht University
    • Harvard Medical School
    • Delta Hospital
    • North Tees and Hartlepool NHS Foundation Trust
    • Irish Coalition for People Living with Obesity
    • Leeds Beckett University
    • KleinePorties

    Research output: Contribution to journalArticlepeer-review

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    Abstract

    The lack of standardization in patient‐reported outcome measures (PROMs) has made measurement and comparison of quality of life (QoL) outcomes in research focused on obesity treatment challenging. This study reports on the results of the second and third global multidisciplinary Standardizing Quality of life measures in Obesity Treatment (S.Q.O.T.) consensus meetings, where a core set of PROMs to measure nine previously selected patient‐reported outcomes (PROs) in obesity treatment research was established. The S.Q.O.T. II online and S.Q.O.T. III face‐to‐face hybrid consensus meetings were held in October 2021 and May 2022. The meetings were led by an independent moderator specializing in PRO measurement. Nominal group techniques, Delphi exercises, and anonymous voting were used to select the most suitable PROMs by consensus. The meetings were attended by 28 and 27 participants, respectively, including a geographically diverse selection of people living with obesity (PLWO) and experts from various disciplines.Out of 24 PROs and 16 PROMs identified in the first S.Q.O.T. consensus meeting, the following nine PROs and three PROMs were selected via consensus: BODY‐Q (physical function, physical symptoms, psychological function, social function, eating behavior, and body image), IWQOL‐Lite (self‐esteem), and QOLOS (excess skin). No PROM was selected to measure stigma as existing PROMs deemed to be inadequate. A core set of PROMs to measure QoL in research focused on obesity treatment has been selected incorporating patients' and experts' opinions. This core set should serve as a minimum to use in obesity research studies and can be combined with clinical parameters.
    Original languageEnglish
    Article numbere13849
    Pages (from-to)(In-Press)
    Number of pages11
    JournalObesity Reviews
    Volume26
    Issue number2
    Early online date17 Oct 2024
    DOIs
    Publication statusE-pub ahead of print - 17 Oct 2024

    Funder

    The S.Q.O.T. II meeting was funded by Medtronic, Johnson and Johnson, Philips Vital Health, Novo Nordisk, Castor, and Bart Torensma. The S.Q.O.T. III meeting was funded by Medtronic, Johnson and Johnson, Novo Nordisk, Goodlife, and Fitforme. The funders of the meeting were not involved in the selection of the PROs or PROMs. None of the members of the S.Q.O.T. organizing committee (PD, CV, VM, BW, IJ, and RL) and none of the participants of the consensus meetings received payment for their participation. Meeting spaces, audiovisual support, catering, travel expenses, and the hotel overnight for the meetings were supported by Johnson and Johnson (S.Q.O.T. II) and Medtronic, Johnson and Johnson, Novo Nordisk, Goodlife, and Fitforme (S.Q.O.T. III). Additionally, the moderator costs (CT) were supported by these sponsors. The sponsors played no role in the selection of participants of the meeting, in the selection of the domains and questionnaires included in this meeting, the voting rounds, or the writing of this paper, nor in any other research related activity. The S.Q.O.T. organizing committee (PD, CV, VM, BW, IJ, and RL) did not receive payment for their work for the S.Q.O.T. initiative.

    Funding

    The S.Q.O.T. II meeting was funded by Medtronic, Johnson and Johnson, Philips Vital Health, Novo Nordisk, Castor, and Bart Torensma. The S.Q.O.T. III meeting was funded by Medtronic, Johnson and Johnson, Novo Nordisk, Goodlife, and Fitforme. The funders of the meeting were not involved in the selection of the PROs or PROMs. None of the members of the S.Q.O.T. organizing committee (PD, CV, VM, BW, IJ, and RL) and none of the participants of the consensus meetings received payment for their participation. Meeting spaces, audiovisual support, catering, travel expenses, and the hotel overnight for the meetings were supported by Johnson and Johnson (S.Q.O.T. II) and Medtronic, Johnson and Johnson, Novo Nordisk, Goodlife, and Fitforme (S.Q.O.T. III). Additionally, the moderator costs (CT) were supported by these sponsors. The sponsors played no role in the selection of participants of the meeting, in the selection of the domains and questionnaires included in this meeting, the voting rounds, or the writing of this paper, nor in any other research related activity. The S.Q.O.T. organizing committee (PD, CV, VM, BW, IJ, and RL) did not receive payment for their work for the S.Q.O.T. initiative.

    Funders
    Medtronic
    Johnson & Johnson
    Philips
    Novo Nordisk
    Castor EDC
    Goodlife
    Fitforme

      UN SDGs

      This output contributes to the following UN Sustainable Development Goals (SDGs)

      1. SDG 3 - Good Health and Well-being
        SDG 3 Good Health and Well-being

      Keywords

      • bariatric surgery
      • obesity treatment
      • patient-reported outcome
      • quality of life

      ASJC Scopus subject areas

      • Public Health, Environmental and Occupational Health
      • Endocrinology, Diabetes and Metabolism

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