The Lullaby Project as a Musical Intervention for Pregnant Individuals With Epilepsy
Primary Purpose
Epilepsy, Pregnancy Related
Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Lullaby Project
Sponsored by
About this trial
This is an interventional supportive care trial for Epilepsy focused on measuring Music, Empowerment
Eligibility Criteria
Inclusion Criteria:
- at least 18 years of age
- currently pregnant and primiparous
- able to provide informed consent
- able to have internet access
- have a confirmed diagnosis of epilepsy based on EEG or clinical evidence
Exclusion Criteria:
- need of a language interpreter to provide informed consent and/or communicate with the MH-RTH musician
- prior involvement in the Lullaby Project
Sites / Locations
- University Health NetworkRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Active Comparator
Arm Label
Control
Lullaby Project
Arm Description
Participants assigned to the intervention group will meet virtually with a professional musician for 5-7 sessions over the course of 10 weeks. Each session will last approximately 1.5 hours and will be conducted via Zoom.
Outcomes
Primary Outcome Measures
Quality of Life in Epilepsy
Assess quality of life related to epilepsy (via QOLIE-31-P, the Patient-Weighted Quality of Life in Epilepsy inventory); minimum value is 0 and maximum value is 100. Higher scores represent better quality of life.
Secondary Outcome Measures
Depression and Anxiety
Assess symptoms of depression and anxiety (via DASS-21, the Depression, Anxiety and Stress Scale - 21 items). Depression scale scores range from 0 to 42 with higher scores representing greater depression severity. Anxiety scale scores range from 0 to 42 with higher scores representing greater anxiety severity. Stress scale scores range from 0 to 42 with higher scores representing greater stress.
Pregnancy-related Empowerment
Assess feelings of empowerment related to pregnancy (via PRES, the Pregnancy-Related Empowerment Scale). Scores range from 16 to 64, with higher scores representing stronger feelings of pregnancy-related empowerment.
Full Information
NCT ID
NCT05503290
First Posted
August 13, 2022
Last Updated
January 30, 2023
Sponsor
University Health Network, Toronto
1. Study Identification
Unique Protocol Identification Number
NCT05503290
Brief Title
The Lullaby Project as a Musical Intervention for Pregnant Individuals With Epilepsy
Official Title
A Pilot Study for the Lullaby Project as a Musical Intervention for Pregnant Individuals With Epilepsy
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 23, 2023 (Actual)
Primary Completion Date
September 1, 2023 (Anticipated)
Study Completion Date
September 1, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Health Network, Toronto
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study's proposed intervention is the randomized participation of pregnant individuals with epilepsy in the Lullaby Project coordinated by a musical institution in Toronto. The purpose of this present study is to investigate the potential benefits of the Lullaby Project on pregnant individuals with epilepsy. Namely, effects on quality of life-related to epilepsy, symptoms of depression and anxiety, perceived stress, and feelings of empowerment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Epilepsy, Pregnancy Related
Keywords
Music, Empowerment
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This study is a randomized-controlled pilot study where enrolled subjects (primiparous individuals with epilepsy) will be randomized 1:1 to the control or intervention group (participation in the Lullaby Project). Outcomes of interest will be measured in each participant at day of consent, 3 weeks after, 7 weeks after, and 10 weeks after. A follow-up via email will be conducted for intervention participants 6 months after their last workshop.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Control
Arm Type
No Intervention
Arm Title
Lullaby Project
Arm Type
Active Comparator
Arm Description
Participants assigned to the intervention group will meet virtually with a professional musician for 5-7 sessions over the course of 10 weeks. Each session will last approximately 1.5 hours and will be conducted via Zoom.
Intervention Type
Behavioral
Intervention Name(s)
Lullaby Project
Intervention Description
Our proposed intervention is the randomized participation of pregnant individuals with epilepsy in the Lullaby Project coordinated by a musical institution in Toronto. The Lullaby Project is an initiative first created by Carnegie Hall's Weill Music Institute. In this program, pregnant women and/or new mothers are paired with professional musicians to compose and write personal lullabies for their child(ren). Since its inception in 2011, the project has expanded globally and have helped numerous families write original lullabies for their newborns. The Lullaby intervention is unlike traditional music therapy as patients are actively participating in the creative song-writing process, not singularly in passive listening. Through sessions, participants will be given an opportunity to share experiences, experiment with musical arrangements, write lyrics, and receive positive feedback from the musician.
Primary Outcome Measure Information:
Title
Quality of Life in Epilepsy
Description
Assess quality of life related to epilepsy (via QOLIE-31-P, the Patient-Weighted Quality of Life in Epilepsy inventory); minimum value is 0 and maximum value is 100. Higher scores represent better quality of life.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Depression and Anxiety
Description
Assess symptoms of depression and anxiety (via DASS-21, the Depression, Anxiety and Stress Scale - 21 items). Depression scale scores range from 0 to 42 with higher scores representing greater depression severity. Anxiety scale scores range from 0 to 42 with higher scores representing greater anxiety severity. Stress scale scores range from 0 to 42 with higher scores representing greater stress.
Time Frame
6 months
Title
Pregnancy-related Empowerment
Description
Assess feelings of empowerment related to pregnancy (via PRES, the Pregnancy-Related Empowerment Scale). Scores range from 16 to 64, with higher scores representing stronger feelings of pregnancy-related empowerment.
Time Frame
6 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
at least 18 years of age
currently pregnant and primiparous
able to provide informed consent
able to have internet access
have a confirmed diagnosis of epilepsy based on EEG or clinical evidence
Exclusion Criteria:
need of a language interpreter to provide informed consent and/or communicate with the MH-RTH musician
prior involvement in the Lullaby Project
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Esther Bui, MD
Phone
416-603-5320
Email
Esther.Bui@uhn.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Sharon Ng, BA
Email
Sharon.Ng@uhnresearch.ca
Facility Information:
Facility Name
University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5T 2S8
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Esther Bui, MD
Phone
416-603-5320
Email
Esther.Bui@uhn.ca
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
The Lullaby Project as a Musical Intervention for Pregnant Individuals With Epilepsy
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