Perioperative Mindfulness Proposal
Feasibility Study to Determine the Effect of Meditation on Perioperative Pain and Distress in Newly Diagnosed Breast Cancer Patients
Hoag Memorial Hospital Presbyterian
24 participants
Jul 31, 2019
INTERVENTIONAL
Conditions
Summary
The purpose of this study is to determine if a regular meditation and breath work practice started before surgery and continued through post-surgical recovery can improve anxiety and pain related to breast cancer and its treatment.
Eligibility
Inclusion Criteria6
- Females 18 years of age or older
- Subject must be able to speak and read English
- Newly diagnosed with primary breast cancer
- Will receive primary surgical treatment for their breast cancer diagnosis.
- Undergoing lumpectomy with or without autologous reconstruction with or without contralateral surgery for symmetry with or without IORT or simple mastectomy without reconstruction
- Breast cancer or DCIS
Exclusion Criteria10
- Recurrent breast cancer
- Current or history of major psychiatric diagnosis.
- Subjects who are receiving neo-adjuvant chemotherapy
- Subjects undergoing modified radical mastectomy or reconstruction
- Subjects regular meditation practice within the past 12 months (defined as greater than twice weekly practice)
- Subjects unwilling or unable to complete study materials or comply with study visits
- Subjects with no access to email or a mobile phone (required to access meditations)
- Subjects undergoing surgery outside Hoag
- Subjects who have narcotic dependence as defined by regular weekly narcotic use before cancer diagnosis.
- Re-excision after lumpectomy (subjects who require re-excision after initial enrollment will be excluded from final analysis and dropped from the study).
Interventions
Two guided meditations will be provided to participants. They will be asked to meditate twice daily, once in the morning once before bed, for a total time of 12 minutes per day. Surgical treatment and postoperative care will be provided by surgeon preference and usual practice, including post-operative pain medications. For 12 weeks patients will maintain a daily meditation log, medication log and complete daily pain assessment questionnaire.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT04049214