Music Intervention for Preoperative Anxiety and Acute Pain Among Mastectomy Patients
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| ClinicalTrials.gov Identifier: NCT04824183 |
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Recruitment Status :
Recruiting
First Posted : April 1, 2021
Last Update Posted : February 25, 2022
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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.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Breast Cancer Mastectomy Pain, Postoperative | Other: Music intervention | Not Applicable |
Show detailed description
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 30 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Intervention Model Description: | Single-blind multicenter randomised controlled trial |
| Masking: | Single (Outcomes Assessor) |
| Primary Purpose: | Supportive Care |
| 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 |
| Actual Study Start Date : | June 5, 2021 |
| Estimated Primary Completion Date : | May 2022 |
| Estimated Study Completion Date : | May 2022 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Music intervention
Music intervention that begins with patient education on WhatsApp will be delivered to participants 3 times within 48 hours before surgery followed by face-to-face monitoring of intervention usage.
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Other: Music intervention
Three WhatsApp sessions will be delivered before the surgery. In the first session, participants will describe their experience with the diagnosis of breast cancer and acceptance. In the second session, participants will be educated on anxiety before their surgery, how anxiety is being managed in the hospital and self-care strategies for anxiety like MI, how to report preoperative anxiety. The third session will include postoperative pain education. The pain education will include information about the type of pain to expect after surgery, medications, pain reporting and MI for pain management. Telephone session; on the day of surgery and at 24 and 48 hours after surgery, a reminder will be sent to the participants by WhatsApp group chat. Face-to-face; MI delivery will involve the delivery of the MP3 to participants and monitoring of their use for 30 minutes both on the day of surgery and 24 and 48 hours after surgery.
Other Name: Hybrid-mode delivered music intervention |
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No Intervention: Usual care
Participants in the control group will receive preoperative pain education via a one-on-one WhatsApp chat. The pain education will focus mainly on the type of pain to expect after surgery, how to report pain and how to request pain medication. MI will not be introduced to the participants in this group neither will there be any phone call for psychological support. Other preoperative care and postoperative care will be provided according to the hospital and ward practices.
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- Change in acute postoperative pain intensity [ Time Frame: Pre-intervention and immediately after the intervention through study completion at 48 hours after surgery ]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
- Change in preoperative anxiety [ Time Frame: Pre-intervention and immediately after the intervention on the day of surgery ]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.
- Change in blood pressure [ Time Frame: Pre-intervention and immediately after the intervention through study completion at 48 hours after surgery ]The systolic and diastolyic blood pressure will be assessed using an automated blood pressure monitor.
- Analgesia consumption [ Time Frame: Post-intervention at 48 hours after surgery ]The type, dosage, frequency and mode administration of analgesia will be assessed and documented in the pharmacological pain prescription and management technique chart.
- Satisfaction with pain management [ Time Frame: Immediately after intervention at 48 hours after surgery ]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
- Change in heart rate [ Time Frame: Pre-intervention and immediately after the intervention through study completion at 48 hours after surgery ]Heart rate will be assessed through an automated machine and documented in beats per minutes
- Change in respiratory rate [ Time Frame: Pre-intervention and immediately after the intervention through study completion at 48 hours after surgery ]Respiratory rate will be counted manually for one full minutes and documented as cycles per minute
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years to 90 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | Female |
| Gender Based Eligibility: | Yes |
| Gender Eligibility Description: | Women aged 18 and above diagnosed with breast cancer and undergoing mastectomy |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria: Women who are:
- Aged 18 years and above
- Diagnosed with breast cancer
- Attending the surgical out-patient clinic for booking visit
- Being scheduled for mastectomy
- Can communicate verbally or in writing in English, Yoruba or Pidgin;
- Without existing chronic pain diagnosis
- 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.
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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): NCT04824183
| Contact: Yetunde O TOLA, Ph.D.(c) | 85254801483 | tolayetunde702@link.cuhk.edu.hk |
| Malawi | |
| Kamuzu Central Hospital | Recruiting |
| Lilongwe, Malawi | |
| Contact: Samuel Bingo, MSc | |
| Principal Investigator: Patrick Phiri, Ph.D | |
| Nigeria | |
| Lagos State University Teaching Hospital | Recruiting |
| Ikeja, Lagos, Nigeria, 23401 | |
| Contact: Njokanma G Iloba, MBBS | |
| Sub-Investigator: Njokanma G Iloba, MBBS | |
| Sub-Investigator: Akinwumi M Lawal, BNSc | |
| Lagos University Teaching Hospital | Recruiting |
| Lagos, Nigeria | |
| Contact: Abdulrasaq Lawal, MBBS | |
| Principal Investigator: Esther O Johnson, BSN | |
| Sub-Investigator: Abdulrasaq Lawal, MBBS | |
| Study Chair: | Ka Ming Chow, DN | The Nethersole School of Nursing, Chinese University of Hong Kong |
| Responsible Party: | Yetunde Oluwafunmilayo TOLA, Principal Investigator, Chinese University of Hong Kong |
| ClinicalTrials.gov Identifier: | NCT04824183 |
| Other Study ID Numbers: |
2021.127 |
| First Posted: | April 1, 2021 Key Record Dates |
| Last Update Posted: | February 25, 2022 |
| Last Verified: | February 2022 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Plan Description: | Individual participant data will not be shared to ensure privacy and confidentiality |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Pain, Postoperative Postoperative Complications Pathologic Processes Pain Neurologic Manifestations |

