Chinese Poem Writing for Improving Mental Wellbeing

March 11, 2026 updated by: Dr Agnes LAI Yuen Kwan, Hong Kong Metropolitan University

Chinese Poem Writing for Improving Mental Wellbeing of Adult Volunteers Serving for People Recovering From Mental Illness

This research proposal aims to explore the impact of poem writing on the well-being of adult volunteers serving patients recovering from mental illness in Hong Kong. The research design was a single-arm intervention study with 30 participants. The intervention consists of two sessions of poem writing, each lasting for 3 hours, led by experienced Chinese teachers or drama directors. The themes of the poems will focus on accomplishment, joy, and gratitude. The primary outcomes are mental well-being and happiness, measured using the Short Warwick-Edinburgh Mental Well-being Scale and a single-item happiness scale. Feasibility outcomes include recruitment rate, retention rate, and acceptability of the interventions. Secondary outcomes include depressive symptoms, anxiety, interest in poem writing, perceived benefits after the activity, and the number of successfully written poems. The proposal also includes plans for in-depth interviews with participants to gather qualitative data. The results will be analyzed descriptively and narratively, with no efficacy statistical tests due to the nature of this feasibility study. The proposal highlights the potential of poem writing as a therapeutic tool for volunteers serving patients recovering from mental illness, enhancing their overall well-being.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

This research proposal aims to explore the impact of poem writing on the well-being of adult volunteers serving patients recovering from mental illness in Hong Kong.The research design was a single-arm intervention study with 30 participants. The intervention consists of two sessions of poem writing, each lasting for 3 hours, led by experienced Chinese teachers or drama directors. The themes of the poems will focus on accomplishment, joy, and gratitude.

The primary outcomes are mental well-being and happiness, measured using the Short Warwick-Edinburgh Mental Well-being Scale and a single-item happiness scale. Feasibility outcomes include recruitment rate, retention rate, and acceptability of the interventions. Secondary outcomes include depressive symptoms, anxiety, interest in poem writing, perceived benefits after the activity, and the number of successfully written poems.

Moreover, the proposal includes plans for in-depth interviews with participants to gather qualitative data. The results will be analyzed descriptively and narratively, with no efficacy statistical tests due to the nature of this feasibility study.

Apart from that, the process evaluation will be done by the instructors after the end of the second class, including the teachers, speakers and the leaders of each group. This act aims to evaluate the effectiveness of using the app in creating and writing poems, as well as the feelings after class on the instructors. An evaluation analysis will be made after the collection of data.

The proposal underscores the potential of poem writing as a therapeutic tool for volunteers serving patients recovering from mental illness, enhancing their overall well-being. Poem writing not only allows volunteers to express their thoughts, emotions, and experiences, but also enhances their self-esteem by validating their feelings and providing a sense of accomplishment. Volunteers working with individuals recovering from mental illness often encounter intense emotions. Writing poems allows them to channel these emotions constructively, preventing burnout and fostering resilience. Furthermore, the act of creating poems can be joyful and fulfilling. Volunteers experience a sense of flow, where time seems to disappear as they immerse themselves in the creative process. Lastly, incorporating poem writing into volunteer programs can be a powerful tool for enhancing both the volunteers' and the patients' well-being, self-esteem, and emotional resilience. Volunteers can find solace, connection, and purpose through their poetic expressions, ultimately benefiting both themselves and the individuals they serve.

Study Type

Interventional

Enrollment (Estimated)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Hong Kong, Hong Kong
        • Recruiting
        • Jockey Club Institute of Healthcare, Hong Kong Metropolitan University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Volunteers serving for people recovering from mental illness or other community residents
  • Aged 18 years old and above
  • Able to understand Cantonese and read Chinese

Exclusion Criteria:

  • Physically or mentally unable to communicate
  • Unwilling to participate or give consent
  • Being involved in other similar activities or research

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Two poem writing sessions
The intervention consists of two sessions of poem writing. Each session lasts for 3 hours. The instructors for each session will include two experienced Chinese teachers or drama directors from Bestreben Drama Association Limited. Adherence to the protocol will be evaluated by two independent reviewers.

The poem themes will focus on accomplishment moments, joyful moments, and gratitude. Participants will be motivated to write at least one poem in each session. The instructor will lead the participants to improve the poem after the participants complete the first draft. The participants will be encouraged to perform in reading their completed poem, sharing their feelings and expressing the meaning of the poems during the session.

In the second session, participants will be invited to do a poem reading performance using one of their newly written poems.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in well-being
Time Frame: Baseline, 2 weeks, 4 weeks, 12 weeks
The 7-item Short Warwick-Edinburgh Mental Well-being Scale with the 5-point Likert scale ("1" means "None of the time", while "5" means "All the time") will be used to measure participants' well-being. The score is calculated by summing up all seven items and with a range of 7 to 35. A higher score indicates a higher positive mental well-being.
Baseline, 2 weeks, 4 weeks, 12 weeks
Changes in happiness
Time Frame: Baseline, 2 weeks, 4 weeks, 12 weeks
Happiness of participants across four timeslots were measured by a single item question, which was "How happy do you think you are" (from "0" = "Not at all" to "10" = "very happy").
Baseline, 2 weeks, 4 weeks, 12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in depressive symptoms
Time Frame: Baseline, 2 weeks, 4 weeks, 12 weeks
The Patient Health Questionnaire (PHQ)-9 will be used to measure depressive symptoms among all participants. Participants rate the frequency of nine symptoms over the past two weeks on a 4-point Likert scale (from "0" = "Not at all" to "3" = "Nearly every day"). The total score ranges from 0 to 27, with higher scores indicating a greater severity of depressive symptoms.
Baseline, 2 weeks, 4 weeks, 12 weeks
Changes in perceived knowledge about limericks (Chinese poem)
Time Frame: Baseline, 2 weeks, 4 weeks, 12 weeks
The changes in participants' perceived knowledge about limericks (Chinese poem) were measured by a single item question, which was "How much do you know about limericks", scoring from "0" (very little understanding) to "10" (very much understanding).
Baseline, 2 weeks, 4 weeks, 12 weeks
Changes in perceived interest in limericks writing
Time Frame: Baseline, 2 weeks, 4 weeks, 12 weeks
The changes in participants' perceived interest in limericks writing were measured by a single item question, which was "How interested are you in limerick writing?", scoring from "0" (very little interest) to "10" (very much interest).
Baseline, 2 weeks, 4 weeks, 12 weeks
Changes in perceived confidence in limericks writing
Time Frame: Baseline, 2 weeks, 4 weeks, 12 weeks
The changes in participants' perceived confidence in limericks writing were measured by a single item question, which was "How confident are you in writing limerick?", scoring from "0" (very little confidence) to "10" (very much confidence).
Baseline, 2 weeks, 4 weeks, 12 weeks
Changes in perceived usefulness of limericks writing
Time Frame: Baseline, 2 weeks, 4 weeks, 12 weeks
The changes in participants' perceived usefulness of limericks writing were measured by three aspects, which were "improving happiness", "improving accomplishment" and "developing new hobbies", all of them were scoring from "0 " (very little help) to "10" (very much help).
Baseline, 2 weeks, 4 weeks, 12 weeks
The number of successfully written poems
Time Frame: 2 weeks, 4 weeks, 12 weeks
The actual number of successfully written poems will be reported subjectively by participants.
2 weeks, 4 weeks, 12 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Recruitment rate
Time Frame: 12 weeks
The percentage of enrolled participants in the approached participants
12 weeks
Retention rate
Time Frame: 2 weeks, 4 weeks
The percentage of adhered participants in the enrolled participants
2 weeks, 4 weeks
Acceptability of the intervention
Time Frame: 2 weeks, 4 weeks
Participants' engagement level (from 0 "did not engage at all" to 10 "totally engaged") and happiness level (from 0 "not at all" to 10 "very happy") after joining the activity, satisfaction towards the activity (from 0 "not at all" to 10 "very satisfied"), willingness to write poems after the activity (from 0 "not at all" to 10 "very willing to") and willingness to attend similar activities in the future (from 0 "not at all" to 10 "very willing to"). An average score will be calculated.
2 weeks, 4 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Agnes YK Lai, Hong Kong Metropolitan University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 13, 2024

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

March 31, 2027

Study Registration Dates

First Submitted

June 13, 2024

First Submitted That Met QC Criteria

August 29, 2024

First Posted (Actual)

September 3, 2024

Study Record Updates

Last Update Posted (Actual)

March 13, 2026

Last Update Submitted That Met QC Criteria

March 11, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • HE-SF2024/19

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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