1. Introduction
Tinnitus denotes the experience of noise or a sound without corresponding acoustic sources [
1]. It is a complex, multifactorial phenomenon, and psychological, audiological, or medical factors can facilitate its onset or maintenance [
2]. Psychological mediators of tinnitus maintenance and tinnitus-related distress include depression [
3], anxiety [
4], as well as perceived stress [
5].
Further, dispositional personality traits can mediate tinnitus-related distress following symptom onset. For example, some patients with chronic tinnitus show higher levels of neuroticism [
6] and lower levels of extraversion [
7]. However, possibly owing to the patient population’s heterogeneity [
8], not all studies suggest personality conspicuities [
9].
Whilst relationships between different psychological factors and the chronic tinnitus experience have been intensively examined in the last years, the exact nature of involved interactions remains unclear. A growing body of qualitative designs set out to investigate individuals’ perceptions of the tinnitus sound and its relation to tinnitus-related distress from a patient’s point of view.
Watts et al. [
10] analysed patients’ free-text responses to investigate why tinnitus was perceived as a problem. Results revealed eight domains of tinnitus-related distress, the most important of which comprised reduced “quality of life”, “fear”, “constant awareness”, “annoyance”, and “inability to concentrate”.
Andersson and Edvinsson [
11] explored the tinnitus experience in subjects involved in psychological treatment for chronic tinnitus. Using semi-structured interviews, the material was analysed following principles inspired by the grounded theory. Their results revealed emotional ambivalence towards tinnitus as a driving force of tinnitus-related distress and three main themes emerged: (1) consequences of tinnitus (mainly negative consequences of living with tinnitus), (2) treatment experience (a summary of treatment experiences in the department of audiology/other providers of care as well as patients’ ambivalence towards knowledge), and (3) tinnitus identity (the ways tinnitus affects one’s private and public identity).
Colagrosso et al. [
12] used qualitative research to assess factors that modulated patients’ individual tinnitus experiences. Using data derived from semi-structured interviews and journal entries, three main themes emerged: (1) participants’ appraisal of their tinnitus, (2) the consequences of tinnitus, as well as (3) environmental and individual factors of attentional focus, stress level, physical state, fatigue, and auditory effort. They identified a dissociation between the tinnitus sensation (i.e., objective loudness, pitch, timbre) and patients’ associated reactions (i.e., perceived loudness, distress) and suggested that this dissociation could potentially have important clinical implications regarding individuals’ ability to cope with the percept.
Pryce and Chilvers [
13] examined notions and interpretations of tinnitus patients regarding the tinnitus symptom, as well as their experience of living with it. Here, qualitative analyses revealed that tinnitus experiences—including the symptom’s acceptance—were influenced by patients’ thinking patterns and “need for sense making”, i.e., rationalising tinnitus and gaining an understanding of its impact on one’s life. The authors postulated that sense making is an important step towards symptom acceptance.
A recently published paper [
14] discussed the burden of illness theory as a framework to understand the allocation of health resources. This theory describes the different ways the health system transfers accountability to patients in order to manage long-term conditions. Using qualitative thematic analysis, the authors examined patients’ accounts of their experiences with living with tinnitus as well as treatments undertaken. Their results showed that the burden of tinnitus could be understood as (1) an effort to cope with the interference of tinnitus in everyday life, as well as (2) behavioural adjustments and modifications that minimise its interference. They additionally identified (3) changes in self-perception after the onset of tinnitus, as well as (4) efforts to integrate those changes in everyday life as relevant characteristics of the burden of tinnitus. The authors proposed that understanding the psychological burden for those living with the condition will further aid the formation of patient-centred interventions.
Dauman and Dauman [
15] interviewed 21 tinnitus patients regarding tinnitus intrusiveness. Using a qualitative analysis method, they identified patterns that influenced tinnitus-induced frustration: (1) searching for perspective on tinnitus, (2) controlling one’s perception despite the tinnitus intrusiveness, and (3) reducing conflicts that arise from social interactions were key patterns which they identified. They incorporated these findings in an empowerment model, which emphasized addressing feelings of frustration and encouraging participation in meaningful activities.
Another qualitative study [
16] set out to investigate attachment style, perceived family support, and tinnitus-related problems. Results demonstrated that avoidant attachment was linked to tinnitus-related problems and that this attachment style was further associated with perceived punitive family responses. The authors argued that these preliminary results could shed further light on the interactions between coping style, perceived support, and tinnitus-related distress.
Erlandsson et al. [
17] used a qualitative design to explore interactions between tinnitus and unique life histories. They interviewed five tinnitus patients using unstructured interviews with free conversation, focussing on the patients’ narrative styles. Their results showed that “regressive” narratives (i.e., including themes suggesting deprivation of basic psychological needs such as autonomy, competence and relatedness) demonstrated an alienation from valued life goals, while “progressive or stable” narratives indicated vitality and orientation in life. They further argued that narrative styles carry important information about patients’ coping styles as well as their resources and should therefore be clinically addressed.
Whilst all above-mentioned studies highlight the importance of investigating individuals’ perceptions and the content of tinnitus-related associations, the studies examined patients’ experiences with tinnitus and patients’ associations induced by tinnitus, regarding tinnitus as a condition, not explicitly as a sound stimulus. This constitutes a gap in our understanding of the interactions between tinnitus as an acoustic phenomenon and linked psychological associations.
The aim of the present pilot study was to explore (1) associations linked to everyday sounds in a group of patients with chronic tinnitus and (2) possible influencing factors of valence ratings. Ten participants (nine of whom provided analysable data) completed a hearing exercise wherein seven neutral auditory stimuli (e.g., a match being lit; applause) were rated as “positive”, “neutral”, or “negative”. In a semi-structured interview, patients’ individual associations with these sounds were further explored. All conversations were transcribed and analysed using Mayring’s qualitative content analysis method.
4. Discussion
The present study set out to qualitatively explore sound-induced psychological associations in a sample of patients with chronic tinnitus. Results indicated three main categories that influenced sound-induced associations: “affective factors”, “factors related to episodic memories”, and “other factors” (i.e., physical discomfort and sensory overload). Our findings suggest that psychological associations induced by neutral auditory stimuli are intricately linked with emotional states that further influence the valence rating and “experience” of those stimuli. Our findings are in line with previous research which demonstrates that auditory stimuli can evoke emotional reactions [
22], which are further central to the perception and categorisation of everyday sounds [
23]. In keeping with a previous study that suggested episodic memories as links between musical experiences and emotional reactions [
24], our analysis further showed that neutral sounds were linked to episodic memories, that is, personal facts and concrete autobiographic information, which, in turn, influenced the sounds’ valence rating. A review investigating how music was associated with memory suggested that music serves as a retrieval cue for autobiographic information and induces memories of associated events [
25]. In line with this suggestion, we propose that everyday sounds likewise serve as retrieval cues and that the autobiographic information that arises influences the subject’s interpretation and valence rating of a neutral sound. A growing body of research has set out to understand the subjective interpretation of sound and the factors that mediate the individual affective response to sounds. Asutay et al. [
26] proposed that individuals react to “auditory events” and argued that apart from the objective characteristics of the sound, both the sound’s context and the listener are integral parameters in any emotional reactions to sounds. In particular, the meaning a listener ascribes to a sound stems from his/her associations and previous experiences. This line of argumentation agrees with our findings, which showed a variety of combinations of different psychological associations and corresponding ratings of the same neutral auditory stimuli. We therefore assume that the rating of a neutral auditory stimulus as pleasant/neutral/unpleasant is mediated by participants’ subjective interpretations of the sound. The above findings could shed light on the different ways tinnitus patients psychologically react to the tinnitus sound.
Previous research has examined the interactions between tinnitus loudness and tinnitus-related distress [
27], as well as mediating factors between perceived loudness and tinnitus-related distress [
28]; future studies should investigate the psychological associations induced by tinnitus as an acoustic stimulus, and the way these associations mediate tinnitus perception and distress. Neuropsychological studies of tinnitus have shown that both acoustic and non-acoustic systems in the brain are involved. Using imaging techniques, increased activity has been measured in both the primary and secondary auditory cortex, as well as in the limbic system and frontal brain [
29]. The activation of brain areas responsible for auditory and cognitive/emotional processing suggests that tinnitus could be understood both as an auditory stimulus and as a psychological retrieval cue. Future studies should explore the subjective interpretation of the tinnitus sound, as well as identify subjective factors that mediate tinnitus perception and its rating.
The present design has several limitations: first, whilst the small sample size might prevent the generalisation of the results, the present study understands itself as an initial exploration of participants’ associations to neutral sounds in a population of patients with chronic tinnitus. Since this paper serves as a proof of concept (PoC) study for upcoming research on possible interactions between tinnitus as an audiological stimulus and underlying affective responses, our main aim was to initially identify psychological factors that mediate the general experience and valence ratings of auditory stimuli in a tinnitus population. Based on the literature concerning the sample size in qualitative designs, the nature of the research question, and the aim of our study, we propose that ten participants offer enough information power for this pilot study design [
30]. Future research will include larger sample sizes.
Moreover, although Mayring’s qualitative content analysis is a methodologically controlled and structured method, subjective interpretation is one of its central components. Therefore, the above-described results necessarily reflect the rater’s subjectivity. Last, the identified sound-induced associations may have been partly biased by the phrasing of the interview questions.
Despite these drawbacks, the present study is the first to explore psychological associations induced by everyday sounds in a sample of patients with chronic tinnitus. Psychodynamic-focused research describes tinnitus as a cry of the soul [
31]. Tinnitus “takes over” the role of the messenger; one could hypothesise that tinnitus has a dual character: a “real” somatic one, as well as a symbolic one. The symbolic meaning of the tinnitus is interconnected with the biography of the individual, and thus cannot be generalised. Therefore, an exploration of the psychological associations induced by the tinnitus sound could potentially enhance our understanding of the ways auditory and psychological parameters interact.
The aim of the study was not to identify similarities and/or differences in the sounds’ effects between a tinnitus population and patients without tinnitus but rather to explore the process of hearing everyday sounds and those sounds’ effects explicitly in a tinnitus population. The present design is not in its nature a case–control, it is much more an initial attempt to explore the process of how everyday sounds are heard and perceived in a tinnitus population. It is not assumed that this process necessarily differs in patients with chronic tinnitus as compared to healthy controls. Rather, the study sets the stage for further studies into how tinnitus sound is linked to autobiographical memories, therefore, opening up potentially important psychological treatment avenues to move the tinnitus sound towards being experienced in a more benign manner. Using a qualitative design and choosing an inductive category development process, we aimed to identify psychological factors that underlie the valence rating of everyday sounds. Furthermore, this is a proof of concept (PoC) study aiming to initially assess aspects of the complex interactions between auditory and affective parameters underlying the valence rating of everyday sounds. Based on our preliminary results, we will prospectively explore how psychoauditive interactions affect the way that tinnitus patients ascribe meaning to the tinnitus sound.
Overall, whilst the qualitative design of the present study bares some limitations, we emphasise the importance of qualitative research to expand our understanding of the tinnitus experience and individuals’ tinnitus interpretations. As proposed by a case study conducted by Dauman and Erlandsson [
32], articulating an individual’s tinnitus experience and forming a coherent narrative may be central to facilitating psychosomatic interactions and positively affect symptom-related distress. The authors additionally stress the clinical importance of understanding tinnitus-related distress from a patient’s point of view and incorporating the patient’s narrative into psychological intervention frameworks.
Furthermore, there is an ongoing shift within evidence-based therapies away from diagnosis-driven interventions and symptom-specific protocols and towards personalised interventions that aim to meet the specific needs of the individual [
33]. To further personalise tinnitus interventions, it is first important to explore and analyse the experiences of tinnitus sufferers and to filter out common denominators. Qualitative research designs enable an in-depth exploration of the subjective experience of living with tinnitus.
To conclude, exploring the subjective interpretation of the tinnitus sound could help us better understand the complex ways patients ascribe meaning to their tinnitus, thus expanding our understanding of the individual’s tinnitus-related distress.