Role of Exposure in Hyperacusis

ConditionHyperacusis
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Hospital, Antwerp

About this trial

This study focuses on patients with a primary complaint of hyperacusis. Hyperacusis has been defined as 'abnormally reduced tolerance to sound'. It shows a high comorbidity with tinnitus, the perception of sound in the absence of a sound source. For the period of one month, hyperacusis and tinnitus severity and exposure to sounds will be evaluated by use of Ecological Momentary Assessment (EMA) in all participants. A novel approach to assessments, EMA prompts participants during their daily life to answer short questionnaires, increasing ecological validity and minimizing the risk for recall and memory biases. At a randomized time point during the one-month period, participants will individually receive a single psychoeducation session (1h) delivered by an experienced audiologist. The goal of the study is to investigate if the psychoeducation session leads to an increase in exposure to sound and a decrease in hyperacusis severity.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

primary complaint of hyperacusis

Disqualifiers

primary complaint of misophonia

primary complaint of tinnitus

undergoing another therapy at the moment of the study

Trial design

Design model

Single group

Treatments tested in this trial

  • Psychoeducation

    Behavioral

    The goal of the psychoeducation session is to provide insight in the hyperacusis symptoms, take away the fear of external noises, and encourage exposure to noise.

Treatment groups

5 Participants
are divided into 1 treatment group
Group A: PsychoeducationExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in EMA questions from baseline to end of the study

Change in questions concerning exposure, hyperacusis and tinnitus during the day from baseline measurement to last day of the study period

Time frame
8 random time points each day during the period of the study, from baseline and after intervention, though study completion for an average of 1 month

Secondary outcomes

1

Hyperacusis Questionnaire

Hyperacusis severity self-report questionnaire, ranging from 0-42 with a higher score representing a higher sensitivity to sounds. A score of 28 is the cut-off for auditory hypersensitivity.

Time frame
before intervention, immediately post intervention
2

Tinnitus Functional Index (TFI)

Tinnitus severity self-report questionnaire, ranging from 0-100 with a higher score representing a more severe tinnitus

Time frame
before intervention, immediately post intervention

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University Hospital, Antwerp

Lead sponsor

Universiteit Antwerpen

Collaborator

This trial is not recruiting at the moment. You can still explore other options: