Music Therapy Video Development in Improving Communication, Emotional Distress, and Recovery in Adolescents/Young Adults Undergoing Treatment for High-Risk Cancer and Their Parents

Malignant Neoplasm Clinical Trial

Official title:

Music Video for AYA-Parent Communication and Resilience

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01556256
• Other study ID #: ANUR1131
• Secondary ID: NCI-2012-00682CD
• Status: Completed
• Phase: N/A
• Start date: April 23, 2012
• Est. completion date: October 2, 2023

Study information

• Verified date: October 2023
• Source: Children's Oncology Group
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This randomized trial studies how well music therapy and parents' education work in improving communication, emotional distress, and recovery in adolescents/young adult patients undergoing treatment for high-risk cancer and their parents. Making a music therapy video may improve communication, emotional distress, and recovery in younger patients undergoing treatment for cancer. It is not yet known whether music therapy and counseling for parents is more effective than information handouts for parents in improving communication and emotional distress in patients undergoing treatment for cancer.

Description:

PRIMARY OBJECTIVES:

I. Compare the efficacy of a Therapeutic Music Video (TMV) intervention with a Therapeutic Music Video plus Parent (TMV+P) intervention on outcomes for adolescents/young adults (AYA) undergoing treatment for high-risk cancer.

II. Compare the efficacy of a TMV intervention with a TMV+P intervention on outcomes for parents of AYA with high-risk cancer.

III. Determine relationships of parent distress and parent perceived family environment with AYA outcomes using a mixed methods approach. (exploratory)

OUTLINE: This is a multicenter study. Patients are stratified according to age in years (11-13 vs 14-17 vs 18-24). Parents are randomized to 1 of 2 intervention arms.

ARM I (TMV, low-dose parent): AYA patients undergo 60-minute sessions, delivered in a private setting during outpatient clinic visits or hospitalizations, within a 6-8 weeks period with board-certified music therapists. The music therapists help patients in brainstorming and lyric writing, singing and creatively exploring how AYA lyrics and structure of the selected music fit together, recording their song with a digital accompaniment track, completing video layout worksheets (determining the contents of the video), taking and gathering photos or making drawings for the video, and viewing clip art and pictures on a computer. The music therapist then digitally formats, compiles, and transfers the AYA-developed music video to a DVD. When completed, the therapist shares the video with the AYA and offers the option of having a video "premiere." AYAs who choose a premiere select a date and time for the viewing and identify individuals they wish to attend (family, friends, healthcare professionals). After the viewing, AYAs receive a copy of their DVD to keep. Parents' presence and involvement during all sessions are directed by the AYAs. Parents receive 2 sessions over 15-60 minutes with a trained study team. During the first session, parents receive handouts of helpful website resources that have specific information to help parents support their AYAs. Team members also assure that parents know how to assess the sites. During the second session, parents receive audio-recorded, telephone-based contact by a trained nurse who asks them questions focusing on the content available on the provided website. The trained nurse also answers any questions parents may have.

ARM II (AYA TMV +P): AYA patients receive intervention as patients in arm I. Parents receive 3 tailored 60-minute sessions with a trained nurse intervener. Sessions are recorded to make sure study nurse delivers the sessions according to the study protocol. Study nurse provides support information to parents using the Robb's Contextual Support Model, including Managing the Chaos: Self Care as the First Step to Caring for Your AYA, Relationship Support: How to Listen to and Encourage Your AYA to Talk; and Strategies for AYA Autonomy Support: Understanding AYA's Ways of Coping. Session 3 content is also based on the Resilience in Illness model. Sessions are also tailored to parents' needs, skills practice and/or role playing, and reflection on and reinforcement of learning. Parents receive written materials on tips and prescribed skills practice plans. AYA and parents complete questionnaires including Illness-Related Distress, Defensive Coping, Spiritual Perspective, Social Integration, Family Environment questionnaires, Hope-Derived Meaning, Self-Transcendence, Positive Coping, Resilience, Parent Distress, and Quality of Life at baseline, at 2 weeks after final session, and then at 90 days after final intervention session. Medical background, intensity of treatment rating scale, and family demographics are also collected.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 124
• Est. completion date: October 2, 2023
• Est. primary completion date: August 31, 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 11 Years to 24 Years

Eligibility

Inclusion Criteria:

• AYA has initial or relapsed cancer diagnosis and is actively on treatment and will continue to be on treatment long enough to complete the intervention and evaluation (4 to 6 weeks)

• AYA meets at least 1 of 3 criteria indicating potentially high palliative care or end-of-life needs:

• Any high-risk cancer (i.e., metastatic or stage IV)

• Receiving moderate- to high-intensity chemotherapy during 3-5 consecutive days in an in- or out-patient setting

• A diagnosis with an estimated 5-year event-free survival of < 50%

• AYA is able to participate in sessions as evaluated by the Karnofsky/Lansky score of 50% or greater

• One consistent parent is willing and available to participate in all parent and evaluation sessions

• AYA is not married and has no children

• AYA and parent are able to read, understand, and speak English

Exclusion Criteria:

• Cancers not usually occurring in childhood/adolescent or young adult populations, such as lung or prostate cancer

• Cognitive impairments that would make it difficult for AYA/parents to participate in the intervention or complete questionnaires (determination in consultation with attending physician, oncologist, and, for adolescents below age 18, the parents)

Related Conditions & MeSH terms

• Malignant Neoplasm
• Neoplasms

Intervention

Other:
• Caregiver-Related Intervention or Procedure
Undergo TMV+P

Procedure:
• Music Therapy
Undergo TMV
• Music Therapy
Undergo TMV+P

Other:
• Quality-of-Life Assessment
Ancillary studies
• Questionnaire Administration
Ancillary studies

Locations

Country	Name	City	State
United States	Children's Healthcare of Atlanta - Egleston	Atlanta	Georgia
United States	Children's Healthcare of Atlanta - Scottish Rite	Atlanta	Georgia
United States	Cincinnati Children's Hospital Medical Center	Cincinnati	Ohio
United States	Cook Children's Medical Center	Fort Worth	Texas
United States	Riley Hospital for Children	Indianapolis	Indiana
United States	Children's Mercy Hospitals and Clinics	Kansas City	Missouri
United States	Children's Hospitals and Clinics of Minnesota - Minneapolis	Minneapolis	Minnesota
United States	University of Texas Health Science Center at San Antonio	San Antonio	Texas

Sponsors (2)

Lead Sponsor	Collaborator
Children's Oncology Group	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	AYA illness-related distress measured by the Mishel Uncertainty in Illness Scale and the McCorkle Symptom Distress scale	The MPLUS software will be used to perform latent variable analysis of covariance (ANCOVA) to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	AYA defensive coping measured by the Jalowiec Coping Scale-Revised	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	AYA spiritual perspective measured by the Reed Spiritual Perspective Scale	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	AYA social integration measured by the Perceived Social Support-Family scale, the Perceived Social Support-Friends scale, and the Perceived Social Support-Health Care Providers	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	AYA family environment measured by the Family Adaptability and Cohesion Scale II	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	AYA family environment measured by the Parent-Adolescent Communication scale	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	AYA family environment measured by the Family Strengths Scale	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	AYA positive coping measured by the Jalowiec Coping Scale-Revised	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	AYA hope-derived meaning measured by the Herth Hope Index	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	AYA self-transcendence measured by the Reed Self-Transcendence scale	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	AYA resilience measured by the Nowotny Confidence subscale, the Haase Resilience in Illness Scale, and the Index of Well-Being	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	Parental distress measured by the Perceived Stress Scale, the Profile of Mood States-Short Form, and the Spielberger's State-Trait Anxiety Inventory-State Component	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	Parent family environment measured by the Family Adaptability and Cohesion Scale	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	Parent family environment measured by the Parent-Adolescent Communication scale	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	Parent family environment measured by the Family Strengths Scale	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	Parent family environment measured by the Perceived Social Support-Health Care Providers	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days
Primary	Parent quality of life measured by the Index of Well-being	The MPLUS software will be used to perform latent variable ANCOVA to account for measurement error and to reduce the number of comparisons.	Up to 90 days