Components analysis of stepped-care CBT for tinnitus: group vs individual treatment effetcs
- Conditions
- Chronic tinnitus
- Registration Number
- NL-OMON23156
- Lead Sponsor
- Maastricht University Faculty of Psychology and Neuroscience
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 6
In order to be eligible to participate in this study, a person must meet all of the following criteria. That is they must:
•Be primarily seeking treatment/help for difficulties caused by subjective tinnitus
•Be at least 18 years of age
•Have at least moderate tinnitus related distress (i.e. TQ score > 30)
A potential participant who meets any of the following criteria will be excluded from participation in this study:
•Severe depression or anxiety as measured by Dutch version of DASS-21.
•Any person who discloses current suicidal intent.
•Currently or undertaken any treatment for tinnitus (e.g. CBT, tinnitus retraining therapy ) within the previous 5 years (including the aforementioned RCT)
•Potential participant has reported to have commenced or ceased a course of antidepressants [i.e. selective serotonin re-uptake inhibitors (SSRIs); selective serotonin and norepinephrine re-uptake inhibitors (SNRIs); atypical antidepressants, tricyclic antidepressants, or monoamine oxidase inhibitors], antipsychotics [Aripiprazole (Abilify), Asenapine (Saphris), Brexpiprazole (Rexulti), Cariprazine (Vraylar), Clozapine (Clozaril), Iloperidone (Fanapt), Lurasidone (Latuda), Olanzapine (Zyprexa), Paliperidone (Invega), Quetiapine (Seroquel), Risperidone (Risperdal), Ziprasidone (Geodon), Haloperidol], anxioltytics [beta blockers, benzodiazepines], Ritalin, hormone replacement therapy, or medication to lower high blood pressure (i.e. thiazide diuretics, ACE inhibitors, angiotensin II receptor blockers, beta blockers, calcium channel blockers, renin inhibitors] within the previous 3 months.
•Currently receiving psychological or any other kind of therapy addressing psychological, social, emotional, and or behavioural problems
•Unable to read and write fluently in Dutch
•Commenced the use of a hearing aid in the previous 3 months
•Has hearing loss greater than 40dB in one or both ears
•Having previously participated in a study from this project.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Tinnitus disability as measured through daily diaries and ecological momentary assessments.
- Secondary Outcome Measures
Name Time Method Tinnitus Functional Inventory (TFI)