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Trial Title:
Purpose in Life Survey
NCT ID:
NCT05790278
Condition:
Breast Cancer
Traumatic Brain Injury
Conditions: Official terms:
Brain Injuries
Brain Injuries, Traumatic
Study type:
Observational
Overall status:
Enrolling by invitation
Study design:
Time perspective:
Prospective
Intervention:
Intervention type:
Other
Intervention name:
Survey
Description:
Completion of a Purpose in Life Survey
Arm group label:
Adults with Early Stage Cancer
Arm group label:
Adults with Traumatic Brain Injury
Arm group label:
Health Control Adults
Summary:
At present, there is no empirical data that specifies the likely prevalence of purpose in
life disruption among various clinical populations. Between one-third and one-half of
cancer survivors report some degree of existential distress during or after their
treatment, but these findings are not specific to the domain of purpose in life.
To address the aforementioned gap, we propose to conduct a survey study to determine the
prevalence of purpose disruption in two clinical populations and determine if the
prevalence of purpose disruption in these populations is different from that of a
normative population.
Criteria for eligibility:
Study pop:
Adults who are either (1) healthy controls, (2) individuals with a qualifying cancer
diagnosis, or (3) individuals with a qualifying Traumatic Brain Injury
Sampling method:
Non-Probability Sample
Criteria:
Inclusion Criteria:
- Age 18+
- Stage 1, 2, 3 cancer
- Cancer types: breast cancer, non-Hodgkin's lymphoma; colorectal cancer
- Receiving oncology services or treatment through AHCI
- Have completed primary cancer treatment within the past 12 months
- Able to communicate in English;
- Able to see and read (with or without assistive devices);
- Has access to a device (computer, phone, tablet) and an email address;
- Access to an internet connection.
- Has a known email address (in EPIC) and/or home telephone number
- Adults who sustained a traumatic brain injury within the past 12 months.
- Attending the 2022 MN State Fair
Exclusion Criteria:
- Have declined consent for use of medical records in research during admission to AH
facility
Gender:
All
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
Accepts Healthy Volunteers
Locations:
Facility:
Name:
Abbott Northwestern Hospital
Address:
City:
Minneapolis
Zip:
55407
Country:
United States
Start date:
August 1, 2022
Completion date:
August 31, 2024
Lead sponsor:
Agency:
Mary Radomski
Agency class:
Other
Source:
Allina Health System
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05790278
