Couple-Based Mindfulness Intervention for Metastatic Colorectal Cancer
- Conditions
- Metastatic Colorectal Cancer
- Registration Number
- NCT05840263
- Lead Sponsor
- University of Colorado, Denver
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 48
Patient Inclusion Criteria:<br><br> - Provision to sign and date the consent form.<br><br> - Stated willingness to comply with all study procedures and be available for the<br> duration of the study.<br><br> - Be aged > 18 years.<br><br> - Fluent in English language<br><br> - Be a person (i.e., patient) diagnosed with metastatic colorectal cancer (mCRC), a<br> partner (e.g., spouse) of someone diagnosed with mCRC, or a clinician who treats<br> patients diagnosed with mCRC.<br><br>Additional patient participant inclusion criteria:<br><br> - Has a current diagnosis of metastatic (Stage IV, recurrent) colorectal cancer<br><br> - Has an ECOG status <2 or otherwise deemed appropriate for study participation by a<br> clinician<br><br> - Is in a committed relationship with a romantic partner for >6 months<br><br> - Has access to computer/internet through with video-conferencing (phone, laptop,<br> tablet, desktop computer)<br><br> - Indicates a score >0 on the Distress Thermometer<br><br>Additional partner participant inclusion criteria:<br><br> - Has been in a committed relationship >6 months with a patient who meets the above<br> eligibility criteria<br><br> - Has access to computer/internet through with video-conferencing (phone, laptop,<br> tablet, desktop computer)<br><br> - Indicates a score >0 on the Distress Thermometer<br><br>Additional clinician participant inclusion criteria:<br><br>·Is a physician or advanced practice clinician (e.g., oncologist, nurse practitioner,<br>physician assistant, psychologist, mental health provider, etc.)<br><br>Exclusion Criteria:<br><br>·Has a serious mental illness (e.g., psychotic disorder), cognitive impairment (e.g.,<br>dementia), or medical condition (e.g., significant impaired sight/hearing) that would<br>compromise participation
Not provided
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Identify the needs of mCRC patients for intervention content;Identify the preferences of mCRC patients for intervention content;Identify the needs of mCRC patients' partners for intervention content;Identify the preferences of mCRC patients' partners for intervention content;Identify the preferences of mCRC patients for intervention format (eg, session length);Identify the preferences of mCRC patients' partners for intervention format (eg, session length);Identify the preferences of mCRC patients partners for intervention format;Extract key themes to integrate into preliminary drafts
- Secondary Outcome Measures
Name Time Method