Interactive Group Drumming (IGD) in Hospital Experience of Patients Undergoing Hematopoietic Stem Cell Transplant - A Pilot Study

NCT ID: NCT03345433

Last Updated: 2020-05-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

35 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-11-15

Study Completion Date

2019-12-04

Brief Summary

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The purpose of this research is to determine if it is possible to perform group drumming as an intervention during HCT, to begin to understand how interactive group drumming during HCT treatment affects patients' well-being (good and bad) during the treatment course and in the first four weeks after completion of the drumming sessions.

Detailed Description

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The purpose of this research is to determine if it is possible to perform group drumming as an intervention during HCT, to begin to understand how interactive group drumming during HCT treatment affects patients' well-being (good and bad) during the treatment course and in the first four weeks after completion of the drumming sessions.

Conditions

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Hematopoietic Cell Transplant

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

interactive group drumming sessions
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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interactive group drumming sessions

Participants will be involved in four interactive group drumming sessions (10-30 minutes each) and complete surveys and questionnaires about music and quality of life.

Group Type EXPERIMENTAL

interactive group drumming sessions

Intervention Type BEHAVIORAL

interactive group drumming sessions

Interventions

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interactive group drumming sessions

interactive group drumming sessions

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* People who are at least 18 years old and are scheduled for HCT
* Individuals must be able to understand and willing to sign a written informed consent form

Exclusion Criteria

* People who are too ill to participate, i.e., while they are in contact isolation or have low platelets (less than 20,000/mcl) will not participate until their condition has improved.
* Patients receiving outpatient HCT except patients with multiple myeloma. Patients with multiple myeloma may participate in the study even though they tend to spend nights away from the hospital.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Wake Forest University Health Sciences

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Richard McQuellon, PhD

Role: STUDY_CHAIR

Wake Forest University Health Sciences

Locations

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Wake Forest University Health Sciences

Winston-Salem, North Carolina, United States

Site Status

Countries

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United States

Provided Documents

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Document Type: Informed Consent Form

View Document

Other Identifiers

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CCCWFU 04417

Identifier Type: OTHER

Identifier Source: secondary_id

IRB00046180

Identifier Type: -

Identifier Source: org_study_id

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