Receptive Music Therapy for the Treatment of Depression

Participants of this study will be recruited through radio and television programs on the topic of depressive symptomatology. The investigators assume that those who are undergoing a cycle of change between a stronger depressive mood and brightened spirits will be more likely to volunteer for study participation than those who are experiencing a period of stronger depressive mood. Consequently, we anticipate an improvement in depressive mood over the study period, even without therapy, for all participants as compared to study entry. To account for this effect, two control groups are included in the study design. Although the anticipated effect size attributable to the specific music is relatively small, depressive symptoms are highly prevalent in the population. Therefore, from a public health perspective, even a small effect on depressive symptomology could make an important contribution to this problem as interventions could be easily designed to be applied in broad circles of the population. Furthermore, the use of specific music may be found to play a role in the future primary prevention of depressive symptoms in the population. Sample size calculation based on on Cohen's d = 0.45. Total target for recruitment = 200 participants. Potential participants will be targeted through advertisements on the radio and television. An internet website will be given during the radio or television advertisement. The website will only contain information about the study and an invitation to participate. Potential participants will be asked to apply by e-mail. The first 500 respondents will be sent a questionnaire in written form. Based on the estimated response rate and inclusion criteria, it is anticipated that 300 invitations for diagnostic interviews will be sent out in response to the received, completed questionnaires after the data has been imported and analyzed. From these 300 invitations, it is estimated that 200 individuals will agree to participation and will be further assessed as meeting the inclusion criteria. These 200 participants will be randomized to the intervention groups (n =100) and both control groups (n = 50 each). Once enrolled in the study, participants will complete an advanced psychometric classification through the use of: * BDI Beck Depression Inventory (Version II), * HADS-D Hospital Anxiety and Depression Scale * SCL-90-R Symptom-Checklist by L.R. Derogatis * STAXI State-Trait Anger Expression Inventory * STAI-G X1 abd X2 State-Trait Anxiety Inventory * TAS-20 Toronto-Alexithymia-Scale * PSQI Pittsburgh Sleep Quality Index * ME Morningness/Eveningness Questionnaire (Horne and Ostberg) * Physiological measurements: heart rate variability measurements