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CompletedNCT03945734Updated Dec 3, 2025

Expressive Helping for Chinese-Speaking Cancer Patients and Survivors

An interventional study of Expressive Helping in Neoplasms and Cancer, sponsored by New York University. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-12-03.

Sponsored by New York University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Not applicable
Ages
18 Years and older
Sex
All
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Study summary

This study examines the feasibility, cultural-sensitivity, and health effects of the expressive helping intervention by conducting a single-arm trial with Chinese-speaking cancer patients and survivors.

Read the detailed description

This study examines whether expressive helping is feasible and culturally-sensitive for Chinese American cancer patients and survivors. For 20 minutes each week over four weeks, participants choose to write or voice-record their thoughts about cancer by following specific prompts designed to help them process their cancer experiences. During the last week of this reflection exercise, participants write or voice-record an anonymous letter to another Chinese cancer patient by sharing their cancer experience and providing advice and encouragement. Health outcomes are assessed at baseline, 1-month, and 3-month follow-ups. A subset of the participants will be invited to share their experiences with the study through qualitative interviews after the last writing/voice-recording session. This research study provides an opportunity for Chinese American cancer patients and survivors to express their feelings without the fear of burdening others, and give them an opportunity to help others by sharing their cancer experiences.

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Conditions studied

  • Neoplasms
  • Cancer

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In context

Neoplasms

9,365 studies on the registry are indexed under Neoplasms; 2,489 are open to participants now.

This study's enrollment of 60 is above the median of 50 across 7,253 interventional studies indexed under Neoplasms.

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Lead sponsor

New York University is the lead sponsor of 120 studies on the registry; 32 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Diagnosis of cancer (any type)
  • Of Chinese descent
  • Over the age of 18
  • Can speaking and read Mandarin Chinese

Exclusion criteria

Exclusion Criteria:

  • Completed primary cancer treatment more than five years ago
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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    Expressive Helping

    Participants complete four 20-minute writing/voice-recording sessions spaced one week apart. During the first week, the instructions will explain that cancer patients and survivors benefit from learning about other cancer survivors' experiences. They are told that the first three weeks of writing/voice-recording (writing/talking about their stress and coping at Week 1, deepest emotions about cancer at Week 2, self-affirmation and benefit finding at Week 3) are exercises designed to help them think about their cancer experiences and to prepare them to write/record the narrative they would share on Week 4. During Week 4, they are asked to write/record a narrative as if they are speaking to another Chinese person with cancer, adding advice and encouragements, and reminded that their writing/recording would be shared with other Chinese American cancer patients and survivors.

    Behavioral: Expressive Helping

Interventions

  • BehavioralExpressive Helping

    Expressive helping harnesses the benefits of helping others (e.g., support giving) through writing or voice-recording. Expressive helping integrates two distinct areas of research showing that writing or speaking about ones' negative experiences and engaging in support giving behaviors can improve psychological well-being.

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What researchers measure

Primary outcomes

  1. Number of participants screened

    The number of participants screened for eligibility will be counted.

    Time frame: through study completion, an average of 1 year

  2. Compliance rate

    Compliance rate is calculated by dividing the number of writing/voice-recording sessions finished by the number of sessions assigned.

    Time frame: through study completion, an average of 1 year

  3. Retention rate

    Retention rate is calculated by dividing the number of participants who began the study by the number of participants who finished the entire study.

    Time frame: through study completion, an average of 1 year

  4. Meaningfulness of the study

    We will ask participants open-ended questions about whether they felt participating in this study was meaningful to them.

    Time frame: This will be assessed approximately four weeks after the baseline

Secondary outcomes

  1. Change in quality of life as assessed by the Functional Assessment of Cancer Therapy Scale (FACT).

    The Functional Assessment of Cancer Therapy Scale (FACT) is a 27-item measure of health-related quality of life (Cella \& Tulsky,1993). This scale assesses contains four different subscales, including physical well-being (7 items), social well-being (7 items), emotional well-being (6 items), and functional well-being (7 items).

    Time frame: Baseline; 1-month follow-up; 3-month follow-up

  2. Change in depressive symptoms as assessed by the Center for Epidemiologic Studies Depression Scale (CES-D).

    The CES-D (Radloff, 1977) is a 20-item measure of depressive symptoms.

    Time frame: Baseline; 1-month follow-up; 3-month follow-up

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Study locations

1 site
  • New York University
    New York, New York 10003, United States
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 3, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03945734
Lead sponsor
New York University
Responsible party
Sponsor
First posted
May 10, 2019
Start date
May 20, 2019
Primary completion
Dec 30, 2020
Completion
Dec 30, 2020
Last update
Dec 3, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2021. You cannot join it, but the record below documents what was studied.

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