Internet-based Versus Face-to-face Clinical Care for Tinnitus
NCT ID: NCT02665975
Last Updated: 2021-07-14
Study Results
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View full resultsBasic Information
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COMPLETED
NA
92 participants
INTERVENTIONAL
2016-08-31
2017-12-31
Brief Summary
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Detailed Description
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Design A two-armed Randomized Control Trial (RCT), will be used to evaluate the effectiveness iCBT on tinnitus distress. Participants placed in the experimental group will receive iCBT and those in the control group will undergo standard face-to-face hospital based clinical care.
Setting: This will be an multi-center study, recruiting from three tinnitus clinics in the East of England, UK; namely: Norfolk and Norwich University Hospital Trust, Milton Keynes University Hospital and Hinchingbrooke Healthcare NHS Trust
Participants: Recruitment will be undertaken from 3 separate clinical settings. Adult patients seen by ENT Consultants or Audiologist at these centers who mention being significantly bothered by tinnitus, and who would normally be referred for tinnitus services will be considered for the study. 80 Participants will be recruited and will be randomly assigned to either receiving face-to-face clinical clinical care consisting or or internet-based intervention (iCBT).
Intervention:
i) iCBT group: This group will undergo a CTB-based internet intervention, providing an opportunity to learn about new ways of coping with tinnitus during everyday life. It is 8 week long e-learning intervention, with new modules introduced weekly and assignments given to practice techniques learnt.
ii) Standard clinical care group: receive individual face-to-face tinnitus appointment providing the care deemed most important to this individual and follow-up appointments as required.
Outcome measures: The main outcome measure is the Tinnitus Functional Index. Secondary outcome measures are the Tinnitus Handicap Inventory- Screening version and self-reported measures for insomnia, hearing disability, cognitive functioning, hyperacusis, anxiety and depression and quality of life. These will be measured at baseline, 3 months post- intervention and 6-months post- intervention, to assess the intervention effects over time.
Hypothesis: If iCBT proves feasible and is effective compared to standard clinical care, it may have implications for the way tinnitus suffers are managed in the UK. It may be that a subset of tinnitus suffers can be managed though an e-learning treatment program, freeing up services for those with more severe problems that need face to face treatment.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Experimental group: iCBT
CBT-based internet-intervention for tinnitus The intervention offered is a CTB-based internet intervention, providing an opportunity to learn about new ways of coping with tinnitus during everyday life. It is 8 week long e-learning intervention, with new modules introduced weekly and assignments given to practice techniques learnt.
CBT-based internet-intervention for tinnitus
Tinnitus e-learning programme
Face-to-face clinical tinnitus care
Receive individual face-to-face tinnitus care, and follow-up appointments as required.
Face-to-face clinical tinnitus care
Hospital tinnitus counselling
Interventions
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CBT-based internet-intervention for tinnitus
Tinnitus e-learning programme
Face-to-face clinical tinnitus care
Hospital tinnitus counselling
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* The ability to read and type in English
* No barriers to using a computer (e.g. significant fine motor control or visual problems)
* Internet and e-mail access, and the ability to use these
* Commitment to completing the programme
* Completion of the online screening and outcome questionnaires
* Agreeing to participate in either group and be randomized to one of these groups
* Understanding and working towards the end goal of reducing the impact and distress of tinnitus, although the strength of the tinnitus may remain the same
Exclusion Criteria
* Reporting pulsatile, objective or unilateral tinnitus, which have not been investigated medically
* Tinnitus as a consequence of a medical disorder, still under investigation
* Undergoing any tinnitus therapy concurrently to partaking in this study
18 Years
ALL
Yes
Sponsors
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Anglia Ruskin University
OTHER
Responsible Party
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Principal Investigators
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Allen Peter
Role: STUDY_CHAIR
Anglia Ruskin University
Locations
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Norfolk and Norwich University Hospital
Norwich, Norfolk, United Kingdom
Hinchingbrooke Hospital
Huntingdon, , United Kingdom
Milton Keynes University Hospital
Milton Keynes, , United Kingdom
Countries
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References
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Rodrigo H, Beukes EW, Andersson G, Manchaiah V. Internet-based cognitive-behavioural therapy for tinnitus: secondary analysis to examine predictors of outcomes. BMJ Open. 2021 Aug 20;11(8):e049384. doi: 10.1136/bmjopen-2021-049384.
Beukes EW, Andersson G, Allen PM, Manchaiah V, Baguley DM. Effectiveness of Guided Internet-Based Cognitive Behavioral Therapy vs Face-to-Face Clinical Care for Treatment of Tinnitus: A Randomized Clinical Trial. JAMA Otolaryngol Head Neck Surg. 2018 Dec 1;144(12):1126-1133. doi: 10.1001/jamaoto.2018.2238.
Beukes EW, Baguley DM, Allen PM, Manchaiah V, Andersson G. Guided Internet-based versus face-to-face clinical care in the management of tinnitus: study protocol for a multi-centre randomised controlled trial. Trials. 2017 Apr 21;18(1):186. doi: 10.1186/s13063-017-1931-6.
Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Document Type: Informed Consent Form
Other Identifiers
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ARU-0116
Identifier Type: -
Identifier Source: org_study_id
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