Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04706728
Other study ID # VEK N-20200038
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 1, 2021
Est. completion date December 2024

Study information

Verified date August 2022
Source Aalborg University
Contact Lars R Bertelsen, PhD. student
Phone +4520406025
Email Larb@hum.aau.dk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess whether music listening is helpful in lowering anxiety in patients about to start their ECT treatment.


Description:

In-patients at a psychiatric hospital referred to ECT treatment, is offered to participate in the study investigating whether listening to expert-curated playlists before-, during and after ECT treatment is helpful as a non-pharmacological intervention in lowering patients anxiety. After written informed consent, participants will be randomised into two groups, one listening to playlists with music, one listening to sounds from nature (e.g. rain, ocean waves). Playlists will be administered by tablet+earphones in the waiting room, tablet+speaker in the room of procedure and tablet+bedside speaker in the recovery room.


Recruitment information / eligibility

Status Recruiting
Enrollment 110
Est. completion date December 2024
Est. primary completion date August 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Capable in-patients of age at Aalborg University Hospital, Psychiatry - departments S7 - S8, diagnosed with unipolar depression, referred to ECT treatment. - patients assessed to fit the study, by the head of departments S7 & S8 - Voluntary participation in the study after written informed consent. - Patients can withdraw their consent at any point during the treatment trajectory. Exclusion Criteria: - Patients not compliant with the study, as assessed by head of departments - Non-capable patients - Patients who withdraw their written informed consent - Patients using hearing aid - Patients with former ECT treatment experience - Patients who receive acute ECT Treatment

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Listening to playlists with music prior to-, during and after the ECT procedure
Patients choose between two expert-curated playlists with music one day prior to ECT procedures for the first four weeks of their ECT treatment.
Listening to playlists with music prior to-, during and after the ECT procedure
Patients choose between two expert-curated playlists with music one day prior to ECT procedures for the first two weeks of their ECT treatment.
Listening to playlists with sound from nature (rain, waves) prior to-, during and after the ECT procedure
Patients choose between two expert-curated playlists with sounds from nature one day prior to ECT procedures for the first two weeks of their ECT treatment

Locations

Country Name City State
Denmark Aalborg University Hospital, Psychiatry Aalborg Region Nordjylland

Sponsors (2)

Lead Sponsor Collaborator
Aalborg University Aalborg University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Other Anxiety Symptom Scale questionnaire (ASS). Defining the type of anxiety.
Validated Anxiety Symptom Scale questionnaire (ASS), measured before 1st., 5th. and 9th. ECT procedure.
First four weeks of treatment.
Other Non/validated questionnaire on patients experience of treatment quality. Self-made questionnaire on patients' experience of the treatment quality using playlists as an add-on to Treatment As Usual (TAU). First four weeks of treatment.
Other Semi-structured Follow-Up interview. Qualitative Follow-Up interview with two participants from each arm, approximately four weeks after their last ECT procedure. One month after last ECT treatment
Primary State-Trait Anxiety Inventory (STAI-Y1) Measurement of patient anxiety before their first-, and before their second ECT procedure.
Patients report of anxiety before their ECT treatment and therefore their anxiety is measured in validated STAI-Y1 questionnaire the evening before the first and before the second ECT procedure.
First week of ECT treatment
Secondary State-Trait Anxiety Inventory (STAI-Y1) Measurement of patient anxiety before their fifth.-, and before their ninth. ECT procedure.
Patients report of anxiety before their ECT treatment and therefore their anxiety is measured in validated STAI-Y1 questionnaire during their first 8 ECT treatments, to see differences in anxiety levels over time (if any).
First four weeks of treatment.
See also
  Status Clinical Trial Phase
Completed NCT05760482 - Evaluation of the Relationship Between Bruxism and Tryptophan Metabolites N/A
Recruiting NCT04368416 - Anxiety/Depression, Sleep and Alcohol in Elderly Anxiety/Depression, Sleep Disturbances and Alcohol Use Disorder in Elderly With Cognitive Complaints
Completed NCT01190774 - Anxiety Assessment Intervention in Dental Patients Phase 2/Phase 3
Not yet recruiting NCT06418269 - The Effect of Therapeutic Play on Anxiety and Fear Levels in Children With Diabetes N/A
Recruiting NCT06215456 - Virtual Reality to Reduce Periprocedural Anxiety During Invasive Coronary Angiography N/A
Completed NCT06114524 - Effect of Binaural Beats on Level of Anxiety and Toleration in Patients Undergoing Upper Gastrointestinal Endoscopy Without Sedation N/A
Completed NCT05316415 - The Effects of Music on the Anxiety and Sleep Quality of Pregnant Women on Bed Rest for a High-risk Pregnancy N/A
Recruiting NCT05433636 - Mindful Waiting Room N/A
Recruiting NCT06034496 - Cranial Electrotherapy Stimulation and Acute Stress N/A
Recruiting NCT06187090 - The Supplementation Therapy in Autism and Response to Treatment Study N/A
Completed NCT05499767 - HEPPI: Efficacy of a Cognitive-Emotional Intervention for Homebound Older Adults N/A
Not yet recruiting NCT03671317 - Medical Clowns for Pediatric Blood Draw N/A
Terminated NCT03227562 - Is Initial Response to Low Dose Risperidone Predictive for Outcome in Anxiety? Phase 3
Completed NCT04040036 - Effects of Virtual Reality on Pain, Fear and Anxiety During Blood Draw in Children Aged 5-12 Years Old N/A
Completed NCT04568551 - COVID-19-associated Anxiety of Pregnant Women for Anomalies, Stillbirth and Preterm Labor
Recruiting NCT06190184 - Viome Precision Nutritional Programs to Improve Clinical Outcomes for Mental Health Conditions N/A
Completed NCT04601545 - The Virtual Reality Therapy as a Pulmonary Rehabilitation Supporting Method N/A
Completed NCT06223412 - Visual Based Program and Climate Change N/A
Recruiting NCT04356638 - a Phase III Trial of Safety and Efficacy of Premedication With Dexmedetomidine and Midazolam in Pediatric Patients Phase 3
Completed NCT03977948 - Qualitative and Systemic Assessment of a Nurse Intervention an Inpatient Child and His or Her Parents