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Behavioural Intervention
Mozart for Anxiety
N/A
Waitlist Available
Led By Dan Drzymalski, MD
Research Sponsored by Tufts Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1-8 hours
Awards & highlights
Study Summary
This trial will study the dose of music listening and types of music to reduce anxiety in C-section patients. Results will be scored pre- and post-music to determine which dose is most effective.
Eligible Conditions
- Anxiety
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1-8 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1-8 hours
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Anxiety Score
Trial Design
2Treatment groups
Active Control
Group I: MozartActive Control1 Intervention
Subjects in this arm will listen to music from a list of pre-selected pieces by Mozart that have been previously shown to have beneficial effects on anxiety.
Group II: Patient preferenceActive Control1 Intervention
Subjects in this arm will listen to music from a list of pre-selected pieces of their own choosing.
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Who is running the clinical trial?
Tufts Medical CenterLead Sponsor
255 Previous Clinical Trials
255,228 Total Patients Enrolled
1 Trials studying Anxiety
21 Patients Enrolled for Anxiety
Dan Drzymalski, MDPrincipal InvestigatorTufts Medical Center
3 Previous Clinical Trials
191 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You should not feel anxious (score 0 out of 10) after giving your consent to participate in the study.You have difficulty hearing.You are regularly taking anxiety medication every day.
Research Study Groups:
This trial has the following groups:- Group 1: Mozart
- Group 2: Patient preference
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
What is the maximum number of patients that can take part in this experiment?
"Affirmative. Clinicaltrials.gov has data that shows this clinical trial is currently accepting applications, which opened on August 7th 2023 and was most recently updated on the 25th of the same month. A total of 66 patients will be accepted across one medical centre."
Answered by AI
Are there any vacancies available in this trial for participants?
"Affirmative. Clinicaltrials.gov attests that this medical study, initially posted on August 7th 2023, is actively seeking volunteers. 66 patients are needed from 1 healthcare facility to complete the trial."
Answered by AI
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