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Tailored multifactorial intervention to improve dizziness symptoms and quality of life, balance and gait in dizziness sufferers aged over 50 years: protocol for a randomised controlled trial
BMC Geriatrics volume 17, Article number: 56 (2017)
Dizziness is a frequently reported symptom in older people that can markedly impair quality of life. This manuscript presents the protocol for a randomised controlled trial, which has the main objective of determining the impact of comprehensive assessment followed by a tailored multifaceted intervention in reducing dizziness episodes and symptoms, improving associated impairments to balance and gait and enhancing quality of life in older people with self-reported significant dizziness.
Three hundred people aged 50 years or older, reporting significant dizziness in the past year will be recruited to participate in the trial. Participants allocated to the intervention group will receive a tailored, multifaceted intervention aimed at treating their dizziness symptoms over a 6 month trial period. Control participants will receive usual care. The primary outcome measures will be the frequency and duration of dizziness episodes, dizziness symptoms assessed with the Dizziness Handicap Inventory, choice-stepping reaction time and step time variability. Secondary outcomes will include health-related quality of life measures, depression and anxiety symptoms, concern about falling, balance and risk of falls assessed with the physiological fall risk assessment. Analyses will be by intention-to-treat.
The study will determine the effectiveness of comprehensive assessment, combined with a tailored, multifaceted intervention on dizziness episodes and symptoms, balance and gait control and quality of life in older people experiencing dizziness. Clinical implications will be evident for the older population for the diagnosis and treatment of dizziness.
The study is registered with the Australia New Zealand Clinical Trials Registry ACTRN12612000379819.
Dizziness is a frequent complaint of older people. Current or chronic symptoms of dizziness are reported by 10% [1, 2] to 30% [3, 4] of community-dwelling older adults with an increasing prevalence as people age [1, 3, 5]. Dizziness markedly impairs quality of life , and is associated with a two-fold increase in the prevalence of self-reported functional disability , worsening of depressive symptoms [2, 4], decreased participation in social activities, poor self-reported health and reduced falls self-efficacy . There is also evidence of a relationship between acute dizziness and falls [3, 7] and the frequency of dizziness episodes is associated with disability , falls and syncopal events .
Dizziness is a subjective sensation that is used to describe feelings such as light-headedness, feeling faint, head spinning, room spinning, unsteadiness, and feeling woozy or giddy. Clinically, dizziness is described as a feeling of altered orientation in space . Traditionally, it has been divided into four main subtypes [9, 10]: (i) vertigo, where patients express illusory sensation of self-motion which often is the result of a vestibular system disorder; (ii) presyncopal dizziness, a light-headed sensation associated with cerebral hypoperfusion; (iii) psychogenic dizziness, associated with a mental health issue such as generalised anxiety; and (iv) disequilibrium and non-specific dizziness, often associated with neuromuscular causes. In older people, dizziness may have a multifactorial aetiology, with many dizzy older patients fulfilling criteria for two or more of the subtypes described above [11–13].
This multifactorial aetiology [11–14] combined with imprecise symptom descriptions , make it difficult to establish an accurate diagnosis of dizziness [16, 17] A retrospective chart audit of 50 older patients with dizziness from a family practice showed that 45% did not have a diagnosis and 10% had more than one diagnosis . Furthermore, in 20% of consecutive older patients presenting to a general practice, there was no attributable cause of dizziness based on clinical characteristics . Other contributing factors to the diagnostic challenge of dizziness include overreliance on symptom description to establish a diagnosis , a tendency to diagnose conditions in the clinicians own field of experience (“the blind men and the elephant” phenomenon) , and the lack of diagnostic accuracy of many tests .
If an accurate diagnosis for the underlying cause of dizziness can be made, there is potential for effective therapy. The Epley manoeuvre and vestibular rehabilitation appear effective in managing Benign Paroxysmal Positional Vertigo (BPPV)  and some unilateral peripheral disorders , respectively. There are also well-established syncope assessment and management guidelines , fall prevention balance and strength exercise programs for older people [24, 25], and emerging cognitive behavioural therapies (CBT) that could be readily applied to older patients with psychogenic dizziness .
A comprehensive multidisciplinary assessment of dizziness holds great promise for more effectively diagnosing and treating dizziness in older people. There have been models proposed before and these have had some success in reducing the number of unresolved cases [5, 9, 13, 14, 27, 28]. However, these assessments are either very time consuming , have never been further developed as tools [13, 27], or are not based on empirical evidence [14, 27, 28]. A one-stop dizziness assessment would be welcomed by older people with dizziness who report that they would like to minimize the number of specialist referrals, for logistical reasons, cost and because they perceive that specialist’s consultations often do not result in successful treatment .
This randomised controlled trial will aim to improve the understanding of dizziness, its assessment and its management in older people, overcoming the barriers we have described. We have designed a comprehensive, multidisciplinary battery of vestibular, cardiovascular, neuromuscular, balance and psychological assessments to improve the likelihood of obtaining a diagnosis for the symptom of dizziness in middle-aged and older people.
To compare the effect of a tailored multifaceted intervention with usual care on frequency of dizziness episodes, balance and gait performance and quality of life in people aged 50 years and over with self-reported significant dizziness.
To establish the cost-effectiveness of the program from the health provider’s perspective.
To determining the effects of the program on vestibular, cardiovascular and psychological measures associated with dizziness.
A single blind parallel group randomised controlled trial will be conducted in 300 participants with dizziness. Figure 1 presents the study flow diagram. The Human Research Ethics Committee of the University of New South Wales approved this study (HC 12152). The study is registered with the Australia New Zealand Clinical Trials Registry (ACTRN12612000379819) (Table 1).
People aged 50 years or older, living in the community will be recruited through advertisements; flyers on community facilities, hospital and university noticeboards; articles in newspapers and newsletters for older people; the Neuroscience Research Australia (NeuRA) website, newsletter and mailing list; and by mail box drops within the local community and retirement villages. To be eligible for the study, participants must: (i) be aged 50 years and over; (ii) have experienced at least one significant episode of dizziness in the past 12 months; (iii) live independently in the community or retirement village and; (iv) be able to understand English. Data will be collected in Australia.
People will be ineligible to participate in the study if they; (i) have a degenerative neurological condition; (ii) are currently receiving treatment for their dizziness; (iii) have a cognitive impairment (a General Practitioner Assessment of Cognition (GPCOG) of <5)  and/or; (iv) are unable to walk 20 m without difficulty with the use of a walking aid.
Participants identified on assessment with conditions that require urgent treatment defined as suspected stroke, transient ischemic attack or other undiagnosed neurological or acute cardiovascular condition, severe depressive or anxiety symptoms will also be excluded from the study and referred following consent for appropriate treatment.
Baseline assessment and case conference
All eligible participants will attend NeuRA for a three-hour baseline assessment undertaken by trained research assistants. The study will be explained in detail and written consent obtained prior to commencing the assessment. The assessments are outlined in Table 2. These include diagnostic tests for descriptive purposes and for allocating intervention participants to treatment arms as well as baseline measures for the primary and secondary outcomes.
A multidisciplinary case conference will then be held within two weeks of the assessment to reach a consensus diagnosis and design a tailored intervention plan based on the baseline assessment results. Results of all assessments undertaken will be reported and recommendations regarding appropriate therapies derived and prioritised. Panel members will include at least a geriatrician, a vestibular neuroscientist, an exercise physiologist and a baseline assessor.
After completion of the baseline assessment and case conference, participants will be randomised into intervention or control groups. Permuted blocks (sizes: 2, 4 and 6) using a computer generated random number schedule will be performed to determine randomisation order. Allocation will be concealed by using central randomisation performed by NeuRA personnel not otherwise involved in the study. Staff performing outcome measurement and data analysis for the primary outcomes will be blinded to group allocation. However, due to the nature of the intervention, it is not possible to blind the staff administering interventions or the participants. Participants will be instructed not to inform the assessors of their intervention status.
Based on their underlying conditions and case conference recommendations, appropriate interventions will be organised for participants assigned to the intervention group (Table 3). The intervention plan will be guided by published normative data for the vision, sensorimotor, balance and psychological tests and the presence of abnormal results in our vestibular and cardiovascular tests. Due to the multifactorial aetiology of dizziness in older people, it is likely that many participants will require multiple interventions which we will implement in a staged manner.
Adverse events (for example, a fall during an exercise session) will be monitored with monthly calendars and telephone calls as required and adherence to all interventions documented with therapist records and/or participant diaries.
A trial safety committee composed of two Senior staff of Neuroscience Research Australia (a Senior scientist and a Senior biostatistician), not involved in any aspect of the study and independent from the sponsor and investigators, will review the withdrawal, deceased and incident data of the trial annually and report to the Ethics Committee.
The control group
Control group participants will receive usual care during the six-month trial period. At completion of the trial, they will be provided with their baseline and re-assessment reports and given the option to being referred appropriate therapies.
Primary and secondary outcomes
The primary outcome measures outlined in Table 2 will capture the four crucial aspects of the trial: dizziness, balance, walking stability and quality of life. The secondary outcome measures, also outlined in Table 2, will elucidate how the interventions assist in ameliorating dizziness symptoms. Dizziness episodes and duration will be ascertained with monthly calendars and telephone calls as required. Participants will return to NeuRA for reassessment of outcomes at the end of the trial (6 months post randomisation). Staff monitoring the dizziness episodes and administering reassessments will be blinded to group allocation.
Sample size calculation
A power analysis determined that 300 participants (150 per group) will need to be recruited to provide 80% power to detect a statistically significant 20% between-group difference in the primary outcome measures. For these calculations, we assumed an alpha of 0.05 and a dropout rate of 15%. We assumed the following control group means (standard deviations), based on values from previous studies of older people [31–33]: choice-stepping reaction time = 1322 (331) ms, step-time variability = 0.02 (0.01) s, and dizziness handicap inventory = 37 (2).
All analyses will use an intention-to-treat approach and analysis of the primary outcomes will be conducted masked to group allocation. Dizziness episodes will be contrasted between groups with negative binomial regression due to the likely Poisson- like distribution of this variable. Between-group comparisons of retest performance for the continuously-scored primary and secondary outcome measures will be made using General Linear Models (ANCOVA) controlling for pre-test performance and other potential confounders. Estimates of the magnitude of clinical improvement in symptoms of anxiety and depression will be derived using calculations of effect size (Cohen’s d) and percentage of symptom improvement. Predictors of uptake, acceptability and adherence will be established using multivariate modelling techniques including multiple linear and logistic regression analyses. Analyses will be conducted using the SPSS software package.
An economic evaluation will be conducted from the perspective of the health and community service provider. Benefits will be measured in terms of quality-adjusted life years (QALY) gained, based on utility weights derived from the EQ-5D and AQoL-6D collected at baseline and at 6 months. The study will collect data on the cost to deliver the intervention program. Using the mean costs in each trial arm, and the mean health outcomes in each arm, the incremental cost per QALY of the intervention group compared to control groups will be calculated and results plotted on a cost-effectiveness plane.
Bootstrap sampling will be used to estimate a distribution around costs and health outcomes, and to calculate the confidence intervals around the incremental cost-effectiveness ratio. We will conduct a one-way sensitivity analysis and a probabilistic sensitivity analysis to estimate the joint uncertainty in cost and effect parameters. A cost-effectiveness acceptability curve will be plotted. A cost-effectiveness acceptability curve provides information about the probability that an intervention is cost-effective, given a decision makers’ willingness to pay for each additional QALY.
This trial is expected to improve our understanding of dizziness by identifying the main contributory causes of this prevalent and debilitating condition in a representative sample of older people. We also hope to demonstrate the efficacy of conducting a comprehensive assessment followed by a tailored multifaceted intervention in reducing dizziness symptoms, improving associated impairments to balance and gait and enhancing quality of life in older people with self-reported dizziness symptoms. If successful, the findings of this trial could be readily translated into clinical practice. The trial also has the capacity to drive the implementation of a profile-based assessment and intervention based on empirical data from quantitative tests that best identify dizziness subtypes.
The outcomes of this study may have important implications, not only for the older population, but also for the general population suffering with dizziness, as it is documented that two percent of adults seek medical attention annually for a new symptom of moderate to severe dizziness or vertigo . Unintended consequences resulting from a sub-optimal assessment of dizziness include multiple referrals to specialists, abandonment of social activities, loss of independence, increased sick leave and job loss, depression and anxiety, falls and concern about falls [1–4, 34, 35]. A validated and multifaceted dizziness profile assessment complemented by evidence-based therapies has the potential to improve individual quality of life across all ages and clinician quality of care, as well as reduce health care and community costs.
This study will determine the impact of a comprehensive assessment followed by a tailored multifaceted intervention in reducing dizziness episodes and symptoms, improving associated impairments to balance and gait and enhancing quality of life in older people with self-reported significant dizziness.
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This trial is funded by an Australian National Health and Medical Research Council (Reference number 1026726). The salaries of KD and SL are funded by Australian National Health and Medical Research Council fellowships. The salary of AAM is funded by a Garnett Passe & Rodney Williams Memorial Foundation Senior Principal Research Fellowship. The research is conducted independently from the funding body.
Availability of data and materials
JM and SL drafted the manuscript. All authors are actively involved in the study. All authors read and approved the final manuscript. SL is the primary study sponsor.
The authors declare that they have no competing interests.
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Ethics approval and consent to participate
The Human Research Ethics Committee of the University of New South Wales approved this study (HC 12152). Written consent was obtained from all participants prior to commencing the study.
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Menant, J.C., Migliaccio, A.A., Hicks, C. et al. Tailored multifactorial intervention to improve dizziness symptoms and quality of life, balance and gait in dizziness sufferers aged over 50 years: protocol for a randomised controlled trial. BMC Geriatr 17, 56 (2017) doi:10.1186/s12877-017-0450-3
- Randomised controlled trial
- Accidental falls
- Postural balance