A CBT-based Internet Intervention for Adults With Tinnitus in the United Kingdom
Primary Purpose
Tinnitus
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
CBT-based internet-intervention for tinnitus
Sponsored by
About this trial
This is an interventional treatment trial for Tinnitus focused on measuring tinnitus treatment, internet-intervention, CBT
Eligibility Criteria
Inclusion Criteria
Participant's eligibility for the study is as follows:
- Aged 18 years and over living in the UK
- 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
- Be available for 12 months after starting the study to complete a 1 year follow-up questionnaire
- Suffering with tinnitus for a minimum period of 3 months
- Tinnitus outcome measure scores indicating the need for tinnitus care (26 or above on the Tinnitus Functional Index)
Exclusion Criteria
- Reporting any major medical or psychiatric conditions
- 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
Sites / Locations
- Vision and hearing Sciences, Anglia Ruskin Univeristy
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
experimental group
weekly check-in group with delayed treatment
Arm Description
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.
will complete weekly measures and commence the treatment once the experimental group completes the intervention
Outcomes
Primary Outcome Measures
The Tinnitus Functional Index
Measure of how severe the tinnitus is Units of measurement: scores on a scale Abbreviation TFI Minimal value: 0 Maximum value 100 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Secondary Outcome Measures
Tinnitus Handicap Inventory-screening Version
Measure of tinnitus severity to use as a weekly measure Measure of how severe the tinnitus is Units of measurement: scores on a scale Abbreviation THI-S Minimal value: 0 Maximum value 40 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Insomnia Severity Index
Measure of sleep problems Measure of how severe the tinnitus is Units of measurement: scores on a scale Abbreviation ISI Minimal value: 0 Maximum value 28 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Cognitive Failures Questionnaire
Measure of how cognitive difficulties such as concentration and memory Units of measurement: scores on a scale Minimal value: 0 Maximum value 100 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Satisfaction With Life
Quality of life measure Units of measurement: scores on a scale Minimal value: 5 Maximum value 35 Higher score is a better outcome Units are scores on a scale Total score used, not sub scales
Patient Health Questionnaire
Measure of signs of depressive disorders Units of measurement: scores on a scale Minimal value: 0 Maximum value 28 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Generalised Anxiety Disorder
Measure of anxiety disorder and traits Units of measurement: scores on a scale Minimal value: 0 Maximum value 21 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Hyperacusis Questionnaire
Measure of abnormal sound sensitivity Units of measurement: scores on a scale Minimal value: 0 Maximum value 42 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Hearing Handicap Inventory- Screening Version
Measure of hearing difficulties or hearing disability using a screening tool Units of measurement: scores on a scale Minimal value: 0 Maximum value 40 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Full Information
NCT ID
NCT02370810
First Posted
February 3, 2015
Last Updated
June 24, 2021
Sponsor
Anglia Ruskin University
Collaborators
Linkoeping University
1. Study Identification
Unique Protocol Identification Number
NCT02370810
Brief Title
A CBT-based Internet Intervention for Adults With Tinnitus in the United Kingdom
Official Title
CBT-based Internet Intervention for Adults With Tinnitus in the United Kingdom: A Randomise Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2021
Overall Recruitment Status
Completed
Study Start Date
January 2016 (Actual)
Primary Completion Date
June 2017 (Actual)
Study Completion Date
September 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Anglia Ruskin University
Collaborators
Linkoeping University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine the feasibility and effectiveness of a CBT-based internet intervention for adults with tinnitus in the United Kingdom
Detailed Description
Objectives Tinnitus is one of the most distressing disabilities and innovative ways of managing the related health care burden is required. A cognitive behavioural therapy (CTB) based internet intervention (iCBT) has been developed in Europe to improve access to tinnitus treatments. This study aims to determine the feasibility and effectiveness of iCBT in reducing the impact associated with tinnitus in the United Kingdom (UK). It furthermore, aims to establish for which subgroups of tinnitus suffers this iCBT intervention would be a suitable intervention.
Design A two-armed Randomized Control Trial (RCT), with a one year follow-up design will be used to evaluate the effectiveness iCBT on tinnitus distress Setting: This will be an internet-based study for adults with tinnitus living in the UK
Participants: Eligible participants will include adults with tinnitus for a minimum period of 3 months with internet access and no major medical or psychiatric conditions. 70 participants will be recruited for each group and will be randomly assigned using a computer generated randomization schedule by an independent research assistant after being pre-stratified for age and tinnitus severity.
Intervention: 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.
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.
Hypothesis: If this intervention proves feasible it is and effective, 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tinnitus
Keywords
tinnitus treatment, internet-intervention, CBT
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
146 (Actual)
8. Arms, Groups, and Interventions
Arm Title
experimental group
Arm Type
Experimental
Arm Description
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.
Arm Title
weekly check-in group with delayed treatment
Arm Type
Other
Arm Description
will complete weekly measures and commence the treatment once the experimental group completes the intervention
Intervention Type
Behavioral
Intervention Name(s)
CBT-based internet-intervention for tinnitus
Other Intervention Name(s)
iCBT
Intervention Description
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.
Primary Outcome Measure Information:
Title
The Tinnitus Functional Index
Description
Measure of how severe the tinnitus is Units of measurement: scores on a scale Abbreviation TFI Minimal value: 0 Maximum value 100 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Time Frame
Assessed at baseline and 8 weeks post-intervention
Secondary Outcome Measure Information:
Title
Tinnitus Handicap Inventory-screening Version
Description
Measure of tinnitus severity to use as a weekly measure Measure of how severe the tinnitus is Units of measurement: scores on a scale Abbreviation THI-S Minimal value: 0 Maximum value 40 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Time Frame
Assessed at baseline and 8 weeks post-intervention
Title
Insomnia Severity Index
Description
Measure of sleep problems Measure of how severe the tinnitus is Units of measurement: scores on a scale Abbreviation ISI Minimal value: 0 Maximum value 28 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Time Frame
Assessed at baseline and 8 weeks post-intervention
Title
Cognitive Failures Questionnaire
Description
Measure of how cognitive difficulties such as concentration and memory Units of measurement: scores on a scale Minimal value: 0 Maximum value 100 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Time Frame
Assessed at baseline and 8 weeks post-intervention
Title
Satisfaction With Life
Description
Quality of life measure Units of measurement: scores on a scale Minimal value: 5 Maximum value 35 Higher score is a better outcome Units are scores on a scale Total score used, not sub scales
Time Frame
Assessed at baseline and 8 weeks post-intervention
Title
Patient Health Questionnaire
Description
Measure of signs of depressive disorders Units of measurement: scores on a scale Minimal value: 0 Maximum value 28 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Time Frame
Assessed at baseline and 8 weeks post-intervention
Title
Generalised Anxiety Disorder
Description
Measure of anxiety disorder and traits Units of measurement: scores on a scale Minimal value: 0 Maximum value 21 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Time Frame
Assessed at baseline and 8 weeks post-intervention
Title
Hyperacusis Questionnaire
Description
Measure of abnormal sound sensitivity Units of measurement: scores on a scale Minimal value: 0 Maximum value 42 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Time Frame
Assessed at baseline and 8 weeks post-intervention
Title
Hearing Handicap Inventory- Screening Version
Description
Measure of hearing difficulties or hearing disability using a screening tool Units of measurement: scores on a scale Minimal value: 0 Maximum value 40 Higher score is a worse outcome Units are scores on a scale Total score used, not sub scales
Time Frame
Assessed at baseline and 8 weeks post-intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria
Participant's eligibility for the study is as follows:
Aged 18 years and over living in the UK
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
Be available for 12 months after starting the study to complete a 1 year follow-up questionnaire
Suffering with tinnitus for a minimum period of 3 months
Tinnitus outcome measure scores indicating the need for tinnitus care (26 or above on the Tinnitus Functional Index)
Exclusion Criteria
Reporting any major medical or psychiatric conditions
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Allen
Organizational Affiliation
Anglia Ruskin University
Official's Role
Study Chair
Facility Information:
Facility Name
Vision and hearing Sciences, Anglia Ruskin Univeristy
City
Cambridge
ZIP/Postal Code
CB1 1PT
Country
United Kingdom
12. IPD Sharing Statement
Citations:
PubMed Identifier
34417217
Citation
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.
Results Reference
derived
PubMed Identifier
29095725
Citation
Beukes EW, Baguley DM, Allen PM, Manchaiah V, Andersson G. Audiologist-Guided Internet-Based Cognitive Behavior Therapy for Adults With Tinnitus in the United Kingdom: A Randomized Controlled Trial. Ear Hear. 2018 May/Jun;39(3):423-433. doi: 10.1097/AUD.0000000000000505.
Results Reference
derived
PubMed Identifier
26399571
Citation
Beukes EW, Manchaiah V, Allen PM, Baguley DM, Andersson G. Internet-based cognitive behavioural therapy for adults with tinnitus in the UK: study protocol for a randomised controlled trial. BMJ Open. 2015 Sep 23;5(9):e008241. doi: 10.1136/bmjopen-2015-008241.
Results Reference
derived
Learn more about this trial
A CBT-based Internet Intervention for Adults With Tinnitus in the United Kingdom
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