- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04957966
Ecological Momentary Music Intervention for the Reduction of Stress
An Ecological Momentary Music Intervention for the Reduction of Stress in the Daily Life of Turkish Immigrant Women
Study Overview
Status
Intervention / Treatment
Detailed Description
The experience of unfair treatment because of one's own ethnicity, i.e., ethnic discrimination, constitutes a complex stressor which triggers both physical and psychological stress reactions. In this regard, women may constitute a particularly vulnerable group, as they may be confronted with intersectional stigmata, i.e., both ethnicity-related and gender-related stigmata. Considering the resulting health impairments many people with migration background are confronted with, it is of great importance to provide interventions with the potential to minimize those negative consequences. Recognizing this necessity, an ecological momentary music intervention was developed in order to reduce psychological and biological (cortisol, alpha-amylase) stress levels due to perceived ethnic discrimination in everyday life. The primary aim of this study is to investigate the feasibility and the effectiveness of this mobile-based intervention.
It is hypothesized that listening to music after an event of acute stress and/or ethnic discrimination will result in stronger decreases in psychological (perceived stress, perceived ethnic discrimination), and biological (cortisol, alpha-amylase) stress levels compared to no music listening in everyday life (immediate effect). Further, it is expected that a decrease in diurnal psychological and biological stress levels will be observed throughout the study period (intermediate effect) and that participants will start to consume or increase their deliberate consumption of music after an event of acute stress and/or ethnic discrimination in their everyday life after the intervention (behavior change). In addition, it is hypothesized that the feasibility of the intervention will be confirmed by participants' self-reports of high usefulness of and satisfaction with the intervention as well as by a high usage rate.
The study design is as follows: Baseline period (week 1), intervention period (week 2 to 4), post period (week 5).
During the baseline and post period, psychological and biological stress fluctuations and perceived ethnic discrimination in daily life will be assessed. To this end, participants will be signaled three times a day (9:00 am, 2:00 pm, 7:00 pm) in order to answer questions on their momentary levels of stress, perceived discrimination, positive and negative affect, and their music-listening activities (time-contingent data entries). Additionally, whenever a stressful or discriminatory event occurs, participants are instructed to initiate a data entry by themselves in order to report their momentary levels of stress, perceived discrimination, positive and negative affect, and to answer questions on the current situation. To investigate activities after such self-initiated, event-contingent data entries, the app will signal the participants 20 (post 1) and 35 minutes (post 2) later for an additional data entry. As part of every time-contingent and event-contingent report, participants will provide a saliva sample in order to examine biological stress markers: salivary cortisol levels as index of hypothalamic-pituitary-adrenal axis (HPA axis) activity, salivary alpha-amylase as index of autonomic nervous system (ANS) activity.
A daily diary assessment will be conducted every evening at the same time. In this diary, participants will be asked about their current perceived stress, perceived discrimination, positive and negative affect, fatigue, coping strategies. Additionally, they will be asked whether discriminatory events had happened over the course of the day and if so, to describe the event(s). For this data entry, no saliva sample will be collected.
During the Intervention period (week 2 to 4), the sampling protocol will be the same as in baseline and post period (i.e., time-contingent data entries, daily diary assessment, self-initiated event-contingent data entries, post 1, post 2). Additionally, after every self-initiated event-contingent report, participants will be randomly assigned (50:50) to either the intervention event (listening to music for 20 minutes) or the control event (no music listening, continue the activity before the data entry). This approach constitutes an intra-individually randomized design.
To investigate the feasibility of the intervention, qualitative data from post-monitoring interviews will be gathered at the end of the study period.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Vienna, Austria, 1010
- University of Vienna
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Turkish immigrants (1st or 2nd generation)
- Weekly ethnic discrimination (at least 2 discriminatory events per week; value of or above 104 on the Everyday Discrimination Scale)
- 18-65 years
- Sex: female
Exclusion Criteria:
- Insufficient proficiency of the German language
- Body mass index (BMI) above 30 kg/m2
- Mental disorders (i.e., current major depressive episode, lifetime psychosis or bipolar disorder, borderline personality disorder, eating disorder in the past 5 years, substance-induced disorder in the past 2 years)
- Chronic somatic diseases
- Medical conditions or medications known to affect endocrine or autonomic functioning
- Abuse of alcohol in the past 6 months
- Drug use in the past year, cannabis use in the past 14 days
- Pregnancy
- Breastfeeding
- Impaired hearing or absolute pitch
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Music listening vs. No music listening
Random assignment (50:50) of every participant to one of the following two conditions: Music listening after a stressful/discriminatory event (i.e., intervention condition) or no music listening after a stressful/discriminatory event (i.e., control condition).
|
20 minutes music listening
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Participants' self-reports on the integrability of the study into the daily life
Time Frame: after 5 weeks
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6 open-ended questions of semi-structured interviews on the integrability of the study into the daily life of the participants
|
after 5 weeks
|
|
Participants' self-reports on the perceived effectiveness of the intervention
Time Frame: after 5 weeks
|
5 open-ended questions of semi-structured interviews on the perceived effectiveness of the intervention
|
after 5 weeks
|
|
Perceived burden regarding the intervention
Time Frame: after 5 weeks
|
10 items of a self-developed questionnaire on perceived burden regarding the intervention (5-point Likert Scales, higher scores indicate greater levels of perceived burden)
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after 5 weeks
|
|
Satisfaction with the intervention
Time Frame: after 5 weeks
|
Combination of the following 10 items to measure participants' satisfaction with the intervention:
|
after 5 weeks
|
|
Usage Rate of the App
Time Frame: Across the 5-week study period
|
Timestamped log-data of the app to determine usage rate by the participants (higher usage rate indicates a greater feasibility of the intervention)
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Across the 5-week study period
|
|
Change in Subjective Stress Experience
Time Frame: from baseline period (week 1) to post period (week 5); during the course of the intervention: T0: directly after a stressful/discriminatory event, T1: after 20 minutes music listening/ not music listening; T2: 15 minutes after T1
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Momentary stress level: visual analogue scales (VAS; 0-100, higher scores indicate a greater level of momentary stress)
|
from baseline period (week 1) to post period (week 5); during the course of the intervention: T0: directly after a stressful/discriminatory event, T1: after 20 minutes music listening/ not music listening; T2: 15 minutes after T1
|
|
Change in Short-Term Neuroendocrine Stress: Hypothalamic-Pituitary-Adrenal Axis
Time Frame: from baseline period (week 1) to post period (week 5); during the course of the intervention: T0: directly after a stressful/discriminatory event, T1: after 20 minutes music listening/ not music listening; T2: 15 minutes after T1
|
Biological Marker: Salivary Cortisol
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from baseline period (week 1) to post period (week 5); during the course of the intervention: T0: directly after a stressful/discriminatory event, T1: after 20 minutes music listening/ not music listening; T2: 15 minutes after T1
|
|
Change in Short-Term Neuroendocrine Stress: Autonomic Nervous System
Time Frame: from baseline period (week 1) to post period (week 5); during the course of the intervention: T0: directly after a stressful/discriminatory event, T1: after 20 minutes music listening/ not music listening; T2: 15 minutes after T1
|
Biological Marker: Salivary Alpha-Amylase
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from baseline period (week 1) to post period (week 5); during the course of the intervention: T0: directly after a stressful/discriminatory event, T1: after 20 minutes music listening/ not music listening; T2: 15 minutes after T1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in participants' behavior regarding music listening
Time Frame: change from baseline period (week 1) to post period (week 5)
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Occurrence of music listening after a stressful/discriminatory event (greater occurrence of music-listening indicates a better outcome)
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change from baseline period (week 1) to post period (week 5)
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Change in positive and negative affect
Time Frame: every evening in the daily diary assessment for 35 days
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PANAS (Positive Affect Negative Affect Scale) is a self-report questionnaire that consists of two scales to measure positive affect and negative affect, each scale consists of 10 items (5-point Likert Scales, for every scale higher scores indicate greater positive/negative affect)
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every evening in the daily diary assessment for 35 days
|
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Change in fatigue
Time Frame: every evening in the daily diary assessment for 35 days
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5 items (one of each scale) of the MFI (Multidimensional Fatigue Inventory), a self-report questionnaire consisting of 20 items that are assigned to 5 scales: general fatigue, physical fatigue, mental fatigue, reduced activity, and reduced motivation (5-point Likert Scales, higher scores on each subscale indicate greater levels of each subscale-specific type of fatigue)
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every evening in the daily diary assessment for 35 days
|
|
Change in coping behavior
Time Frame: every evening in the daily diary assessment for 35 days
|
5 items of the Brief-COPE (Coping Orientation to Problems Experienced), a self-report questionnaire that consists of 28 items to measure effective and ineffective ways of coping with stressful life events; one item of each subscale: active coping, use of emotional support, use of instrumental support, venting, religion; 5-point Likert-Scales with higher scores for each subscale indicating a greater level of the subscale-specific coping behavior)
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every evening in the daily diary assessment for 35 days
|
|
Change in avoidance behavior regarding discriminatory events
Time Frame: every evening in the daily diary assessment for 35 days
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Combination of the following 4 items to measure change in avoidance behavior:
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every evening in the daily diary assessment for 35 days
|
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Change in anticipation of discriminatory events
Time Frame: every evening in the daily diary assessment for 35 days
|
3 items of the Racism-related Vigilance Scale, a 6-item scale to measure heightened vigilance regarding discriminatory events (5-point Likert-Scales with higher scores indicating greater levels of anticipation of discriminatory events)
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every evening in the daily diary assessment for 35 days
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ricarda Nater-Mewes, Dr. Dr., University of Vienna
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- EMMI-T Pilot
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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