Hubei University of Science and Technology
Xianning, Hubei, 437000, China
NCT Number: NCT06917170
Interventional Trial (Randomized Experimental Design)
Study Goal:
This clinical trial aims to evaluate the effectiveness of a structured music therapy program in improving mental health (depression, anxiety, stress) and self-efficacy among college students.
Key Questions the Study Aims to Answer:
Does music therapy significantly reduce symptoms of depression, anxiety, and stress in college students?
Does music therapy significantly enhance self-efficacy in college students?
How do improvements in mental health relate to changes in self-efficacy?
Study Design:
Researchers will compare outcomes between two groups:
Experimental Group: Receives a 2-week daily music therapy intervention (1 hour per session) in a controlled environment.
Control Group: Does not receive any music therapy intervention during the study period.
Participant Activities:
Complete pre- and post-intervention assessments using validated scales:
Depression-Anxiety-Stress Scale (DASS-21) to measure mental health status.
Self-Efficacy Scale to evaluate confidence in personal capabilities.
Experimental group participants will:
Engage in daily music therapy sessions featuring rhythmically smooth and soothing music selected to promote relaxation.
Experience the intervention in a quiet, controlled environment.
Control group participants will:
Continue their regular routines without any therapeutic intervention.
All participants will submit responses via electronic questionnaires (Wenjuanxing platform) to ensure efficient and accurate data collection.
Duration:
Intervention Period: 2 weeks.
Data Collection: Pre-intervention baseline assessment, immediate post-intervention assessment.
Looking for future studies?
Notify Me18 year–25 year
All sexes
Interventional
Not applicable
Xianning, Hubei, 437000, China
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
1.Participants who are unable to fully participate in the 2-week intervention (such as dropping out midway or taking leave) or who do not complete the pre- and post-intervention questionnaires will be excluded.
Description:
Content: Participants engage in passive music therapy sessions where they listen to pre-selected music with smooth rhythms and harmonies (e.g., classical, ambient, or instrumental tracks). The music is chosen to align with evidence-based criteria for promoting relaxation and emotional regulation.
Frequency: Daily (1 session/day).
Duration: 1 hour per session, for a total of 14 sessions over 2 weeks.
Setting: Conducted in a quiet, controlled environment to minimize external distractions.
Goal: To reduce symptoms of psychological distress (depression, anxiety, stress) and enhance self-efficacy through auditory stimulation and emotional engagement.
Time frame: 2 weeks
The assessment was conducted using the simplified version of the Depression Anxiety and Stress Scale. The full scale consists of 21 items, with each of the three subscales (depression, anxiety and stress) containing 7 items. All items are scored on a 4-point scale ranging from "0" (not applicable) to "3" (always applicable). The scores of each subscale are multiplied by 2 to obtain the score of that subscale. The higher the score, the more likely it is to indicate the presence of such emotions.
Hubei University of Science and Technology
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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