Expressive Writing Program Among Young Adults With Blood Cancer
An Expressive Writing Program to Support Emotional Wellness Among Young Adults With Hematologic Malignancy
1 other identifier
interventional
100
1 country
1
Brief Summary
The goal of this study is to learn more about an expressive writing workshop among people with blood cancer. The main question it aims to answer is whether and how an expressive writing workshop can impact mental wellness. Participants will
- Take part in an online expressive writing workshop for four weeks
- Take three surveys at different times over 12 weeks Researchers will compare changes in mental wellness reported by the participants of the workshop to those who will wait four weeks to start the workshop. After four weeks, the participants who are waiting will start their workshop.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2026
CompletedFirst Submitted
Initial submission to the registry
February 10, 2026
CompletedFirst Posted
Study publicly available on registry
February 17, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 30, 2026
May 7, 2026
February 1, 2026
8 months
February 10, 2026
May 1, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Mental Wellbeing
Participants' mental wellbeing will be evaluated using the Warwick Edinburgh Mental Wellbeing Scale (WEMWBS), specifically the original 14-item scale developed by researchers at the University of Warwick and the University of Edinburgh in 2007. This self-report questionnaire asks questions about participants' feelings and how they have been functioning over the last two weeks to capture a comprehensive view of their recent mental wellbeing. Participants will rate each question on a 5-point Likert scale, and their responses will be totaled to a mental wellbeing score ranging from 14-70; higher scores indicate greater wellbeing.
Baseline, 4, and 8 weeks
Perceived Stress
A self-report questionnaire captures whether participants perceive different life situations as overwhelming or uncontrollable. Participants will rate each question on a 5-point Likert scale, and their responses will be totaled to a stress score ranging from 0-40, with higher score indicated more perceived stress.
Baseline, 4, and 8 weeks
Study Arms (2)
Group 1
EXPERIMENTALPrimary Intervention Group
Group 2
PLACEBO COMPARATORWait List Control Group
Interventions
Group 1 will start the workshop the following week. Group 2 will wait 4 weeks before starting the workshop. There is an equal chance of being placed group 1 or group 2. You cannot choose your study group. The workshop is the same for both groups.
Eligibility Criteria
You may qualify if:
- Patient with a hematologic malignancy diagnosis in treatment or after treatment is completed, who is currently between the ages of 18 and 39 (young adult), or the informal caregiver of a young adult blood cancer patient
- Located within the U.S., Canada, or U.S. territories
- Able to read and write in English
You may not qualify if:
- Located outside of the U.S., Canada, or its territories
- Participant is a minor aged 17 years or below
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Blood Cancer United
Washington D.C., District of Columbia, 20005, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 10, 2026
First Posted
February 17, 2026
Study Start
February 1, 2026
Primary Completion (Estimated)
September 30, 2026
Study Completion (Estimated)
September 30, 2026
Last Updated
May 7, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share
Participant data will be shared at the aggregate, deidentified level only.