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Depression in Visual Impairment Trial (DEPVIT): A Randomized Clinical Trial of Depression Treatments in People With Low Vision

  • Claire L. Nollett
  • , Nathan John Bray
  • , Catey Bunce
  • , Robin J. Casten
  • , Rhiannon Edwards
  • , Mark T. Hegel
  • , Sarah Janikoun
  • , Sarah E. Jumbe
  • , Barbara Ryan
  • , Julia Shearn
  • , Daniel J. Smith
  • , Miles Stanford
  • , Wen Xing
  • , Tom H. Margrain
    • School of Healthcare Sciences, Cardiff University
    • National Institute for Health Research Biomedical Research Center (NIHR BRC) for Ophthalmology at Moorfields Eye Hospital NHS Foundation Trust London
    • UCL Institute of Ophthalmology, London
    • Dartmouth College, Hanover, NH, USA
    • Ophthalmology (Eye) Department South Wing, St. Thomas' Hospital, London
    • University of South Wales
    • Institute of Health and Wellbeing, University of Glasgow, Glasgow, Scotland
    • National Institute for Social Care and Health Research (NISCHR)
    • Thomas Jefferson University, PA

    Allbwn ymchwil: Cyfraniad at gyfnodolynErthygladolygiad gan gymheiriaid

    255 Wedi eu Llwytho i Lawr (Pure)

    Crynodeb

    Purpose: The purpose of this study was to compare two interventions for depression, problem solving treatment (PST) and referral to the patient's physician, with a waiting-list control group in people with sight loss and depressive symptoms.
    Methods: This was an assessor-masked, exploratory, multicenter, randomized clinical trial, with concurrent economic analysis. Of 1008 consecutive attendees at 14 low-vision rehabilitation centers in Britain, 43% (n = 430) screened positive for depressive symptoms on the Geriatric Depression Scale and 85 of these attendees participated in the trial. Eligible participants were randomized in the ratio 1:1:1 to PST, referral to their physician, or a waiting-list control arm. PST is a manualized talking intervention delivered by a trained therapist who teaches people over six to eight sessions to implement a seven-step method for solving their problems. Referral to the physician involved sending a referral letter to the person's physician, encouraging him or her to consider treatment according to the stepped care protocol recommended by the U.K.'s National Institute of Health and Care Excellence. The primary outcome was change in depressive symptoms (6 months after baseline) as determined by the Beck Depression Inventory.
    Results: At 6 months, Beck Depression Inventory scores reduced by 1.05 (SD 8.85), 2.11 (SD 7.60), and 2.68 (SD 7.93) in the waiting-list control, referral, and PST arms, respectively. The cost per patient of the PST intervention was £1176 in Wales and £1296 in London.
    Conclusions: Depressive symptoms improved most in the PST group and least in the control group. However, the change was small and the uncertainty of the measurements relatively large.
    Iaith wreiddiolSaesneg
    Tudalennau (o-i)4247-4254
    CyfnodolynInvestigative Ophthalmology & Visual Science
    Cyfrol57
    Dynodwyr Gwrthrych Digidol (DOIs)
    StatwsCyhoeddwyd - 31 Awst 2016

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