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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05790278
Other study ID # 1920306
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date August 1, 2022
Est. completion date August 31, 2024

Study information

Verified date February 2024
Source Allina Health System
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 300
Est. completion date August 31, 2024
Est. primary completion date August 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

Other:
Survey
Completion of a Purpose in Life Survey

Locations

Country Name City State
United States Abbott Northwestern Hospital Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mary Radomski

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Purpose Status Question A single forced-choice self-report screener question that we developed in order to characterize existential distress related to purpose in life (PSQ: "Related to living with purpose in life, right now I am: moving backwards; stalled; figuring it out; moving forward on a path"). Through Study Completion, about 15 minutes
Secondary Work and Adjustment Scale A 5-item self-report questionnaire to characterize functioning related to work, social life, leisure, home management, and relationships. Through Study Completion, about 15 minutes
Secondary Meaning in Life Questionnaire A 10-item questionnaire designed to measure 2 dimensions of meaning in life: Presence of Meaning (how much respondents feel their lives have meaning) and Search for Meaning (how much respondents strive to find meaning and understanding in their lives). Through Study Completion, about 15 minutes
Secondary Life Engagement Test A 6-item self-report questionnaire that captures the extent to which a person engages in activities that are personally valued. Through Study Completion, about 15 minutes
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