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.
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页数:10
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