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A Prospective Randomized Controlled Study on the Treatment of Breast Cancer Patients with Anxiety and Depression via Guided Music Imagination Combined with Singing Technique

A Prospective Randomized Controlled Study on the Treatment of Breast Cancer Patients with Anxiety and Depression via Guided Music Imagination Combined with Singing Technique

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000991
Enrollment
Unknown
Registered
2026-04-16
Start date
2026-04-25
Completion date
Unknown
Last updated
2026-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast cancer with anxiety and depression

Interventions

Control Group:Routine Treatment
Intervention Group:On the basis of routine treatment, receive group music therapy 3 times a week, each session includes guided music imagination and song singing techniques. And need to practice guide

Sponsors

Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18-70 years old, female; (2) Clinically diagnosed with breast cancer (stage II, III, IV), and confirmed to have comorbid anxiety and/or depression, with the severity meeting any of the following criteria: 1) Hamilton Anxiety Scale score = 7 and = 13; 2) and/or Hamilton Depression Scale score = 8 and = 19; (3) Expected survival period of more than 1 year; (4) After resection or radical operation, or no indication for cancer surgery during enrollment; (5) No central nervous system metastasis, no obstacles in language communication and comprehension ability; (6) No use of anti-anxiety and/or anti-depressant psychiatric drugs in the past month, except for benzodiazepines and melatonin receptor agonist hypnotics; (7) Patients with stable vital signs, clear consciousness, and able to receive music therapy and follow-up visits regularly; (8) Voluntarily participate in the study and sign the informed consent form after the researcher explains the purpose of the study.

Exclusion criteria

Exclusion criteria: A subject will be excluded if he/she meets any of the following criteria: (1)Complicated with severe cardiovascular and cerebrovascular diseases, respiratory system diseases, such as acute cerebral infarction, severe chronic obstructive pulmonary disease, liver cirrhosis, etc.; (2)Suffering from acute infectious diseases or acute exacerbation of chronic diseases, such as acute hepatitis, acute attack of asthma, etc.; (3)Subjects with known or suspected poor compliance who cannot complete the trial, such as alcoholism, drug dependence, mental illness, severe visual and hearing impairment, or illiteracy, and those judged by the researcher as unsuitable to participate in this clinical trial; (4)People who dislike music; (5)Other reasons that the researcher deems unsuitable for participating in this trial.

Design outcomes

Primary

MeasureTime frame
Hamilton Anxiety Scale Score;Hamilton Depression Scale Score;

Secondary

MeasureTime frame
Pittsburgh Sleep Quality Index;Patient Quality of Life Measurement Scale;Traditional Chinese Medicine Syndrome Score;Respiratory Rate;Self-Rating Depression Scale Score;Blood Pressure;Self-Rating Anxiety Scale Score;Heart Rate;

Countries

China

Contacts

Public ContactWangzixin

Guangzhou Medical University, Xinzao Town, Panyu District, Guangzhou City, Guangdong Province

songfenghuangui@163.com15820235078

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: May 1, 2026