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Clinical Trials/NCT06286332
NCT06286332Not yet recruitingNot Applicable

The Effectiveness of Music Therapy on Fatigue and Laboratory Values in Acute Leukemia Patients Undergoing Chemotherapy

Chang Gung University1 site in 1 country60 target enrollmentStarted: March 1, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
60
Locations
1
Primary Endpoint
Change from baseline in fatigue on the Tang Fatigue Rating Scale (TFRS) and 11-point Numeric Rating Scale (NRS-11) at day 21.

Study Overview

Brief Summary

The objective of this study is to assess the efficacy of employing music therapy in alleviating fatigue and medical laboratory values among patients with acute myeloid leukemia.

Detailed Description

The researchers will explain the study objectives and methods, obtain informed consent, and have participants sign the consent form before commencing the study. Participants are randomly assigned to Group A and Group B. Participants in Group A undergo 30 minutes of self-selected music playback every day in addition to receiving standard therapy, while participants in Group B only receive standard therapy. The entire study duration spans 21 days.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Double (Care Provider, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Diagnosed with acute myeloid leukemia by a clinical specialist.
  • •Patients undergoing chemotherapy for the first time.
  • •Aged 18 years or older, capable of communicating in Mandarin or Taiwanese.
  • •Normal hearing ability.
  • •No history of psychiatric disorders and clear consciousness.
  • •Participants with no prior involvement in any intervention studies related to fatigue management.
  • •Demonstrates understanding of the research objectives, willingly participates in the study, and completes the informed consent form.
  • •Willing to cooperate with study procedures throughout the research period.

Exclusion Criteria

  • •Severe hearing impairment.
  • •Individuals with unstable vital signs or altered consciousness.

Arms & Interventions

Music Therapy

Experimental

Participants received self-selected music app playback for 30 minutes every day and standard therapy. The entire study duration spans 21 days.

Intervention: Music Therapy (Other)

Standard Care

No Intervention

Participants only received standard care during the entire study duration span of 21 days.

Outcomes

Primary Outcomes

Change from baseline in fatigue on the Tang Fatigue Rating Scale (TFRS) and 11-point Numeric Rating Scale (NRS-11) at day 21.

Time Frame: Baseline and Day 21.

The TFRS and NRS-11 is validated, self-reported instrument assessing average fatigue intensify. The TFRS comprises a total of 37 items, encompassing 15 questions related to physiological aspects, 12 questions addressing psychosocial factors, and 10 questions focusing on daily living activities. The scoring system ranges from 1 to 10, with higher scores indicating a greater level of fatigue. NRS-11 scores range from 0 (no fatigue) to 10 (worst possible fatigue). Change = (Day 21 score - Baseline score).

Secondary Outcomes

  • Change from baseline in neutrophil, hemoglobin, abumin at day 21.(Baseline and Day 21.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Chien-Yu Wu

Nurse

Chang Gung University

Study Sites (1)

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