Breast Cancer Clinical Trial
Official title:
A Pilot Study on the Effect of Culturally-adapted Music Intervention on Preoperative Anxiety and Acute Postoperative Pain Among African Women Undergoing Mastectomy: A Randomised Controlled Trial
NCT number | NCT04824183 |
Other study ID # | 2021.127 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 5, 2021 |
Est. completion date | March 27, 2022 |
Verified date | August 2022 |
Source | Chinese University of Hong Kong |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Anxiety is a common thing that patients experience when they are preparing to have a surgery. When this anxiety is not properly treated, the patients tend to consume more drugs in the operating room and it also cause their pain to increase after surgery. Pain after surgery is common among patients who have just had surgery. The pain that women who have had mastectomy feels after surgery is usually treated using pain killers. Yet, the pain killers are not enough to reduce the pain or cause some unwanted outcomes for the patients. Therefore, supplementing pain killers with music therapy appears to be a good way to reduce the pain and the unwanted outcomes that may arise from taking too much pain killers. This research is aimed to test how effective music that is selected by patients, considers their culture and psychological needs can be helpful in reducing anxiety before surgery and pain after surgery. Also its effect on blood pressure, breathing rate and pulse will be tested. The researcher also hope to know how satisfied patients who consent to participate in the study are with their pain management. The study will be done in two Nigerian hospitals and will mainly include women who have cancer, are above the age of 18, scheduled to have mastectomy, can read or write English or Pidgin, without any mental health challenge and agrees to participate in the study. This study hope to enrol up to 112 women and put them into two groups randomly, one group will receive the music intervention and the other group will receive the normal care provided by the hospital. Participants in the music intervention group will be added to a WhatsApp group on the week of their surgery. The WhatsApp session will be three times within the week of the surgery and each session will be about 30 minutes long. This study will use a combination of very short videos and voice notes (3 minutes) as well as real time chats and pictures to enhance communication on the group chat. The researcher will initiate discussions about participant's experience with breast cancer diagnosis, teach them about anxiety before surgery and pain after surgery. Then, they will ask questions that will be answered and also choose their type of music and send it to the group. The songs will be downloaded into a device and given to them on the day of surgery. They will continue to listen to the music after their surgery for the next two days. Before participants receive the music on the day of surgery, anxiety level and vital signs will be assessed. After the surgery, participant's pain level, vital signs and satisfaction with pain management before and after the intervention will be assessed. Those in the second group will receive a one-on-one chat with the researcher about pain after surgery. For all the participants, the study will be completed two days after the surgery.
Status | Completed |
Enrollment | 36 |
Est. completion date | March 27, 2022 |
Est. primary completion date | March 22, 2022 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 90 Years |
Eligibility | Inclusion Criteria: Women who are: 1. Aged 18 years and above 2. Diagnosed with breast cancer 3. Attending the surgical out-patient clinic for booking visit 4. Being scheduled for mastectomy 5. Can communicate verbally or in writing in English, Yoruba or Pidgin; 6. Without existing chronic pain diagnosis 7. Consent to join the study. - Exclusion Criteria: 1. Pre-existing mental health disorders and cognitive impairment if they are 2. Transferred to the intensive care unit due to complications within the first two days after surgery. - |
Country | Name | City | State |
---|---|---|---|
Malawi | Kamuzu Central Hospital | Lilongwe | |
Nigeria | Lagos State University Teaching Hospital | Ikeja | Lagos |
Nigeria | Lagos University Teaching Hospital | Lagos |
Lead Sponsor | Collaborator |
---|---|
Chinese University of Hong Kong |
Malawi, Nigeria,
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* Note: There are 13 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in acute postoperative pain intensity | The Visual Analogue Scale will be used to assess the pain intensity level. The score on this scale ranged from 0 to 10, higher score represents high pain intensity | Pre-intervention and immediately after the intervention through study completion at 48 hours after surgery | |
Secondary | Change in preoperative anxiety | Spielberger State-Trait Anxiety Inventory will be used to assess anxiety level. This is a four point likert scale with score ranging from 0 to 80. Higher score represents high anxiety level. | Pre-intervention and immediately after the intervention on the day of surgery | |
Secondary | Change in blood pressure | The systolic and diastolyic blood pressure will be assessed using an automated blood pressure monitor. | Pre-intervention and immediately after the intervention through study completion at 48 hours after surgery | |
Secondary | Analgesia consumption | The type, dosage, frequency and mode administration of analgesia will be assessed and documented in the pharmacological pain prescription and management technique chart. | Post-intervention at 48 hours after surgery | |
Secondary | Satisfaction with pain management | Patient satisfaction with pain management will be assessed using the numerical rating scale. The score on this scale ranged from 0 to 10, higher score represents high level of satisfaction | Immediately after intervention at 48 hours after surgery | |
Secondary | Change in heart rate | Heart rate will be assessed through an automated machine and documented in beats per minutes | Pre-intervention and immediately after the intervention through study completion at 48 hours after surgery | |
Secondary | Change in respiratory rate | Respiratory rate will be counted manually for one full minutes and documented as cycles per minute | Pre-intervention and immediately after the intervention through study completion at 48 hours after surgery |
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