Virtual Poetry Workshops to Enhance Patient Well Being and Reduce Anxiety
Poetry Workshops to Enhance Patient Well-Being and Reduce Anxiety Levels
1 other identifier
interventional
80
1 country
1
Brief Summary
This study examines whether participating in poetry workshops can improve emotional well-being among patients with chronic digestive symptoms. Many individuals with long-standing digestive conditions experience distress, anxiety, isolation, and difficulty expressing their emotions in clinical settings. These emotional challenges can negatively affect daily life, relationships, and overall health. Poetry writing offers a creative and supportive way for participants to explore their feelings, express their experiences, and build emotional resilience. It also allows individuals to focus on aspects of their identity beyond their illness. The purpose of this research is to evaluate whether poetry workshops can reduce anxiety, lessen feelings of isolation, and strengthen participants' sense of community and well being. 1\. Why is this study being done? The purpose of this research study is to offer a creative outlet for patients to explore their identity and story, build resilience, and seek hope. This study is being done because we understand that the psychological discomfort that can come upon hearing a diagnosis can lead to increased anxiety levels, negatively impacting a patient's well-being and relationships. Often healthcare practitioners may merely view a patient through the lens of their diagnosis, neglecting other aspects of their identity and humanity. Through reading various poems, crafting their own poems, and sharing their work with their peers, we hope the workshops offer a comforting opportunity for the participants to explore their identities and creativity.
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 Jul 2026
Typical duration 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
First Submitted
Initial submission to the registry
July 16, 2026
CompletedStudy Start
First participant enrolled
July 17, 2026
CompletedFirst Posted
Study publicly available on registry
July 21, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 16, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2028
July 21, 2026
July 1, 2026
2 years
July 16, 2026
July 16, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Change in Anxiety and Depression Symptoms
Assessed using the HADS questionnaire
Between baseline and 8 weeks after start of poetry sessions
Change in Dyspepsia Symptoms
This will be assessed using electronic questionnaire that asks them to rate dyspepsia symptoms on a scale from None- Very severe
Assessed from Baseline to end of poetry sessions (8 weeks)
Study Arms (2)
Experimental group
EXPERIMENTALParticipants selected for the facilitated poetry workshop will meet once a week for approximately 1.5 hours via Zoom. Before each workshop, participants will complete a survey evaluating their general emotional state. Each session will begin with a 10-minute warm-up relating to the workshop's theme to ease the participants into the workshop and to cultivate a comfortable environment for the participants to discuss with one another. The warmup will be followed by the facilitator reading a poem and a discussion of the poem. This discussion will pertain to the participants' initial thoughts and emotions upon hearing the poem. Afterwards, participants will have the opportunity to craft their own poem and share their art with their fellow participants. The workshop will close with a final reading of the poem by one of the participants. At the end of each workshop, patients will complete a survey evaluating their emotional state,
Control Group
ACTIVE COMPARATORParticipants will be provided with a manual with the selected poems, reflection questions, and writing prompts. In accordance with the 8-week schedule followed by the facilitated poetry workshops, participants in the control group will partake in each of the 8 workshops and complete the surveys outside of the scheduled virtual group sessions. The last workshop will be conducted in an interview-style format. After every two workshops, a member of the research team will call each participant to check in on their progress.
Interventions
participants will have the opportunity to craft their own poem and share their art with their fellow participants. This will be facilitated by one of the research team members who will help them craft their own poem.
Participants will receive a written manual that will guide them on how to write poetry. they will receive one manual each week.
Eligibility Criteria
You may qualify if:
- At least 18 years old
- Ability to provide informed consent
- Able to speak and understand English
- Able to attend virtual poetry workshops
- Willing to share at least 3 poems at the end of the study with the study team
- Have access to a high-speed internet connection and smart phone or computer
- Willing to participate in group activity if randomized to the facilitated workshops
- At least moderate dyspepsia assessed by the Dyspepsia questionnaire (at least one of the following symptoms with moderate or worse severity- nausea, vomiting, early satiety, post prandial fullness AND
- At least moderate anxiety or depression assessed by HADS questionnaire. The HADS score has 2 subscores- HADS-A for anxiety and HADS-D for depression. A score of ≥ 21 indicates moderate anxiety and will be required to be eligible for the study.
You may not qualify if:
- Unable to speak English or participate in virtual sessions
- Younger than 18 years old
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ohio State University Wexner Medical Center
Columbus, Ohio, 43210, United States
Related Publications (3)
Gaillard R, Mir O. Fluoxetine and motor recovery after ischaemic stroke. Lancet Neurol. 2011 Jun;10(6):499; author reply 500-1. doi: 10.1016/S1474-4422(11)70111-9. No abstract available.
PMID: 21601157BACKGROUNDLee B, Mafi J, Patel MK, Sorensen A, Vangala S, Wei E, Sarkisian C. Quality improvement time-saving intervention to increase use of a clinical decision support tool to reduce low-value diagnostic imaging in a safety net health system. BMJ Open Qual. 2021 Feb;10(1):e001076. doi: 10.1136/bmjoq-2020-001076.
PMID: 33579745BACKGROUNDBarrett E, Dickson M, Hayes-Brady C, Wheelock H. Storytelling and poetry in the time of coronavirus. Ir J Psychol Med. 2020 Dec;37(4):278-282. doi: 10.1017/ipm.2020.36. Epub 2020 May 14.
PMID: 32406356BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Subhankar CHAKRABORTY, MD, Ph.D.
Ohio State University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 16, 2026
First Posted
July 21, 2026
Study Start
July 17, 2026
Primary Completion (Estimated)
July 16, 2028
Study Completion (Estimated)
December 31, 2028
Last Updated
July 21, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share
Due to privacy concerns, we cannot share IPD