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Study of a Support Program for Quality of Life in Chinese Cancer Patients and Survivors

A Multicomponent Support Program to Enhance Quality of Life in Chinese Cancer Patients and Survivors (MSP-CCS): Pilot Optimization Trial and Implementation Outcomes

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07454330
Enrollment
64
Registered
2026-03-06
Start date
2026-02-27
Completion date
2028-02-01
Last updated
2026-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Survivorship

Keywords

Chinese, Quality of Life, Patients, Survivors, 26-025

Brief summary

The purpose of this study is to evaluate different combinations of cancer education sessions, counseling sessions, and peer support meetings developed for Chinese cancer patients and survivors. The researchers will look at whether the combinations are practical and effective, and how they impact participants' quality of life.

Interventions

Cancer Education on side effects and their management, treatment options, advance care planning, and survivorship. Each session will last about 30-60 minutes and will be completed over the phone or by video call.

OTHERMeaning-Centered Counseling

Meaning-centered counseling aims to activate culturally relevant meaning-focused coping strategies in Chinese-speaking patients and survivors (CCS). Each session will last about 45-60 minutes and will be completed over the phone or by video call.

OTHERPeer Support

Peer support aims to increase social support for CCS to decrease cancer stigma, which has been associated with greater psychological distress, especially among less acculturated Chinese immigrant CCS. The meetings will include up to 6-8 Mandarin-speaking patients and survivors and will last about 90 minutes.

enhanced standard care ( written cancer information materials in Chinese and referral to counseling)

Sponsors

Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER
American Cancer Society, Inc.
CollaboratorOTHER
Brooklyn College Cancer Center
CollaboratorUNKNOWN
Herald Cancer Association
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Using a 2x2x2 factorial design. Participants will be randomized to receive a combination of one or more culturally tailored telehealth-delivered intervention components.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosed with cancer (any type/stage) (per EMR for MSK patients or self-report for external participants) within the last 5 years * Age ≥ 18 years (per EMR for MSK patients or self-report for external participants) Self-Report Criteria: * Of Chinese descent * Speaks Mandarin "well" or "very well" * Moderately low HRQOL (\<70 FACT-G score)4, 48 * Resides in New York or New Jersey * Agrees to participate via telehealth (video or phone) * Agrees to be audio-recorded

Exclusion criteria

Self-Report Criteria: * Per PI determination, requires a higher level of care for current passive or active suicidal ideation than current protocol is able to provide. If a participant receives a score of \> 0 on item 9 of the PHQ-9,5 they will be referred to study PI for further evaluation using the Columbia-Suicide Severity Rating Scale. They will be excluded from participation in this study if there is presence of suicidal risk, determined by affirmative response(s) on the Columbia-Suicide Severity Rating Scale (C-SSRS) * Too ill to participate determined by the question: "Do you feel too ill to participate because of communication problems, uncontrollable pain, or other symptoms that prevent you from participating?" * Cognitive impairment (Montreal Cognitive Assessment 5 Minute - telephone version with a score \< 12) * Per consenting professional determination, unable to understand the informed consent procedure * Participation in study #14-076: Adaptation of Individual Meaning-Centered Psychotherapy for Chinese immigrant cancer patients) * Currently receiving/have received psychotherapy/counseling/peer support within the last 6 months (patients being treated solely with psychotropic medications will not be excluded if they are not receiving psychotherapy/counseling/peer support)

Design outcomes

Primary

MeasureTime frameDescription
Proportion of eligible participants who enroll in the trial.2 years
Proportion of participants who complete treatment24 weeksPproportion of assessments that are completed, with completion defined as submitting the 24-week assessment with a minimum of the FACT-G completed.

Countries

United States

Contacts

CONTACTFlorence Lui, PhD
luif@mskcc.org646-888-8375
CONTACTJennifer Leng, MD, MPH
646-888-8057
PRINCIPAL_INVESTIGATORFlorence Lui, PhD

Memorial Sloan Kettering Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026