Protocol for a randomised controlled feasibility study of psychologically informed vestibular rehabilitation for people with persistent dizziness: INVEST trial

被引:6
|
作者
Herdman, David [1 ,2 ]
Norton, Sam [1 ]
Pavlou, Marousa [3 ]
Murdin, Louisa [4 ,5 ]
Moss-Morris, Rona [1 ]
机构
[1] Kings Coll London, Inst Psychiat Psychol & Neurosci, Hlth Psychol Sect, London, England
[2] St Georges Univ Hosp NHS Fdn Trust, London, England
[3] Kings Coll London, Ctr Human & Aerosp Physiol Sci, London, England
[4] Guys & St Thomas NHS Fdn Trust, London, England
[5] UCL, Ear Inst, London, England
基金
美国国家卫生研究院;
关键词
Protocol; Feasibility; Dizziness; Vertigo; Vestibular; Rehabilitation; CBT; PPPD; COGNITIVE-BEHAVIORAL THERAPY; CHRONIC SUBJECTIVE DIZZINESS; VISUAL VERTIGO; ANXIETY; RESPONSIVENESS; PREDICTORS; RECOVERY; NEURITIS; VALIDITY; SCALE;
D O I
10.1186/s40814-021-00896-y
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Dizziness is a common complaint that often persists and leads to disability and distress. Several cognitive and behavioural responses may contribute to the neurobiological adaptations that maintain persistent vestibular symptoms. This paper will present the protocol of a two-arm parallel group feasibility randomised controlled trial designed to determine whether a fully powered efficacy trial is achievable by examining the feasibility of recruitment, acceptability and potential benefits of an integrated cognitive behavioural therapy and vestibular rehabilitation (CBT-VR) treatment for people with persistent dizziness. Methods: Forty adult patients will be recruited from a tertiary vestibular clinic with persistent movement-triggered dizziness for 3 months or longer who have moderate-high levels of dizziness handicap. Participants will be 1:1 randomised, using a minimisation procedure, to six sessions of either CBT-VR (intervention arm) or VR only (control arm). Measures will be collected at baseline and 4 months post randomisation. The primary feasibility outcomes include descriptive data on numbers meeting eligibility criteria, rates of recruitment, numbers retained post randomisation, treatment adherence and an acceptability questionnaire. Treatment effects on self-report outcomes will be estimated to determine that 95% confidence intervals for the effects are consistent with anticipated effects and minimum clinically important differences, and to provide information needed for the power calculation of an efficacy trial. A nested qualitative study will be conducted post-intervention (intervention group only) to explore the acceptability of the intervention and identify any areas in need of improvement. Discussion: If a trial of CBT-VR is feasible, acceptability data will be used to enhance the intervention if needed and refine the multicentre RCT protocol. Future studies will need to consider the training required for other physiotherapists to deliver the intervention.
引用
收藏
页数:10
相关论文
共 50 条
  • [21] INdividual Vocational and Educational Support Trial (INVEST) for young people with borderline personality disorder: study protocol for a randomised controlled trial
    Andrew M. Chanen
    Katie Nicol
    Jennifer K. Betts
    Gary R. Bond
    Cathrine Mihalopoulos
    Henry J. Jackson
    Katherine N. Thompson
    Martina Jovev
    Hok Pan Yuen
    Gina Chinnery
    Judith Ring
    Kelly Allott
    Louise McCutcheon
    Ashleigh P. Salmon
    Eoin Killackey
    Trials, 21
  • [22] ReaDySpeech for people with dysarthria after stroke: Protocol for a feasibility randomised controlled trial
    Mitchell C.
    Bowen A.
    Tyson S.
    Conroy P.
    Pilot and Feasibility Studies, 4 (1)
  • [23] A multi-centre randomised controlled trial of rehabilitation aimed at improving outdoor mobility for people after stroke: Study protocol for a randomised controlled trial
    Pip A Logan
    Mat P Leighton
    Marion F Walker
    Sarah Armstrong
    John R F Gladman
    Tracey H Sach
    Shirley Smith
    Ossie Newell
    Tony Avery
    Hywel Williams
    James Scott
    Kathleen O’Neil
    Annie McCluskey
    Simon Leach
    David Barer
    Claire Ritchie
    Ailie Turton
    Jane Bisiker
    David Smithard
    Tess Baird
    Paul Guyler
    Therese Jackson
    Ingrid Watmough
    Maggie Webster
    Janet Ivey
    Trials, 13
  • [24] A multi-centre randomised controlled trial of rehabilitation aimed at improving outdoor mobility for people after stroke: Study protocol for a randomised controlled trial
    Logan, Pip A.
    Leighton, Mat P.
    Walker, Marion F.
    Armstrong, Sarah
    Gladman, John R. F.
    Sach, Tracey H.
    Smith, Shirley
    Newell, Ossie
    Avery, Tony
    Williams, Hywel
    Scott, James
    O'Neil, Kathleen
    McCluskey, Annie
    Leach, Simon
    Barer, David
    Ritchie, Claire
    Turton, Ailie
    Bisiker, Jane
    Smithard, David
    Baird, Tess
    Guyler, Paul
    Jackson, Therese
    Watmough, Ingrid
    Webster, Maggie
    Ivey, Janet
    TRIALS, 2012, 13
  • [25] Cognitive Rehabilitation for Attention and Memory in people with Multiple Sclerosis: study protocol for a randomised controlled trial (CRAMMS)
    Lincoln, Nadina B.
    das Nair, Roshan
    Bradshaw, Lucy
    Constantinescu, Cris S.
    Drummond, Avril E. R.
    Erven, Alexandra
    Evans, Amy L.
    Fitzsimmons, Deborah
    Montgomery, Alan A.
    Morgan, Miriam
    TRIALS, 2015, 16
  • [26] Cognitive Rehabilitation for Attention and Memory in people with Multiple Sclerosis: study protocol for a randomised controlled trial (CRAMMS)
    Nadina B. Lincoln
    Roshan das Nair
    Lucy Bradshaw
    Cris S. Constantinescu
    Avril E. R. Drummond
    Alexandra Erven
    Amy L. Evans
    Deborah Fitzsimmons
    Alan A. Montgomery
    Miriam Morgan
    Trials, 16
  • [27] Evaluation of two electronic-rehabilitation programmes for persistent knee pain: protocol for a randomised feasibility trial
    Groves-Williams, Dawn
    McHugh, Gretl A.
    Bennell, Kim L.
    Comer, Christine
    Hensor, Elizabeth M. A.
    Conner, Mark
    Nelligan, Rachel K.
    Hinman, Rana S.
    Kingsbury, Sarah R.
    Conaghan, Philip G.
    BMJ OPEN, 2022, 12 (06):
  • [28] Facet-joint injections for people with persistent non-specific low back pain (FIS): study protocol for a randomised controlled feasibility trial
    Harbinder Sandhu
    David R. Ellard
    Felix Achana
    James H. L. Antrobus
    Shyam Balasubramanian
    Sally Brown
    Melinda Cairns
    Frances Griffiths
    Kirstie Haywood
    Charles Hutchinson
    Ranjit Lall
    Stavros Petrou
    Nigel Stallard
    Colin Tysall
    David A. Walsh
    Martin Underwood
    Trials, 16
  • [29] Facet-joint injections for people with persistent non-specific low back pain (FIS): study protocol for a randomised controlled feasibility trial
    Sandhu, Harbinder
    Ellard, David R.
    Achana, Felix
    Antrobus, James H. L.
    Balasubramanian, Shyam
    Brown, Sally
    Cairns, Melinda
    Griffiths, Frances
    Haywood, Kirstie
    Hutchinson, Charles
    Lall, Ranjit
    Petrou, Stavros
    Stallard, Nigel
    Tysall, Colin
    Walsh, David A.
    Underwood, Martin
    TRIALS, 2015, 16
  • [30] ASSERT (Acute Sacral inSufficiEncy fractuRe augmenTation) randomised controlled, feasibility in older people trial: a study protocol
    van Berkel, Dawn
    Ong, Terence
    Drummond, Avril
    Hendrick, Paul
    Leighton, Paul
    Jones, Matthew
    Salem, Khalid
    Quraishi, Nasir
    Brookes, Cassandra
    Di Paola, Ana Suazo
    Edwards, Sarah
    Sahota, Opinder
    BMJ OPEN, 2019, 9 (07):