The Effects of Music Therapy as a Complementary Intervention in the Treatment of Pediatric Asthma
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| ClinicalTrials.gov Identifier: NCT02201836 |
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Recruitment Status :
Completed
First Posted : July 28, 2014
Last Update Posted : July 28, 2014
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Asthma | Other: One time music therapy Other: Group music therapy | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 200 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Triple (Participant, Care Provider, Investigator) |
| Primary Purpose: | Supportive Care |
| Official Title: | The Effects of Music Therapy as a Complementary Intervention in the Treatment of Pediatric Asthma |
| Study Start Date : | January 2006 |
| Actual Primary Completion Date : | January 2012 |
| Actual Study Completion Date : | January 2012 |
| Arm | Intervention/treatment |
|---|---|
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Active Comparator: One time music therapy session
One time music therapy session which consists of music meditation, including as assessment/evaluation of confined body breathing function as expressed through drawing and coloring post music imagery session. This is followed by an entrainment wind playing/breath expansion music therapy intervention. At the end of the session, the subjects are given a donated wind instrument for play at home.
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Other: One time music therapy |
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Active Comparator: Weekly group music therapy intervention
The weekly group music therapy intervention consists of children and teens using guided visualization and expressing their fears and or fantasies related to breathing with one another. This is followed by creative music improvisations with part-playing on flutes, slide whistles, recorders and melodicas.
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Other: Group music therapy |
| No Intervention: Control |
- Quality of Life [ Time Frame: 6 months ]The Juniper Questionnaire is a stringent quality of life measure that provides interview for children and teens and their parents. It is one of the few scales that requires these interviews to occur separately, so that children and parents do not feel compelled to answer what they think the other desires to hear. We also used take home journals and a comprehensive medical assessment to learn of ER visits, missed school days, avoidance of medication, and allergens in the home, as well as socio-economic status - these factors are known in the literature to effect outcomes and exacerbations with this population.
- Increase volume capacity [ Time Frame: 6 months ]Spirometry enabled us to analyze the possible effects of wind playing on the child's breathing
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| Ages Eligible for Study: | 7 Years to 18 Years (Child, Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- between the ages of 7 and 18
- diagnosed with asthma
Exclusion Criteria:
- over 18
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02201836
| United States, New York | |
| Beth Israel Medical Center | |
| New York, New York, United States, 10003 | |
| Principal Investigator: | Joanne Loewy, DA | Beth Israel Medical Center |
| Responsible Party: | Beth Israel Medical Center |
| ClinicalTrials.gov Identifier: | NCT02201836 |
| Other Study ID Numbers: |
142-04 |
| First Posted: | July 28, 2014 Key Record Dates |
| Last Update Posted: | July 28, 2014 |
| Last Verified: | July 2014 |
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Asthma Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases |
Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity Immune System Diseases |

