← Back to Clinical Trials
Recruiting NCT07789093

NCT07789093 Coaching in Palliative Surgical Oncology

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07789093
Status Recruiting
Phase
Sponsor Singapore General Hospital
Condition Palliative Care
Study Type INTERVENTIONAL
Enrollment 220 participants
Start Date 2026-03-24
Primary Completion 2028-03-30

Eligibility & Interventions

Sex All sexes
Min Age 21 Years
Max Age 99 Years
Study Type INTERVENTIONAL
Interventions
CONCORD coaching intervention

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 220 participants in total. It began in 2026-03-24 with a primary completion date of 2028-03-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study aims to evaluate the effectiveness of a serious illness coaching intervention (CONCORD) in improving quality of serious illness conversation (SIC), treatment decision-making, goal-concordant care delivery and quality of life in patients with advanced cancer considered for palliative interventions. CONCORD will be delivered by lay healthcare providers. We compare outcomes between participants receiving CONCORD vs usual care.

Eligibility Criteria

Inclusion Criteria: (i) Patient: 1. Aged 21 or above; 2. Diagnosis of advanced cancer, i.e. stage 3 or 4 solid organ 3. Consulted for palliative surgery or other interventions, i.e. procedures aimed at relieving symptoms and improving quality of life 4. Able to speak English or Mandarin; (ii) Caregiver 1. Aged 21 or above; 2. Self-endorsed or identified by the enrolled patient as an unpaid spouse/partner, relative or friend who knows them well and who provides regular care, who does not have to live in the same dwelling 3. Able to speak English or Mandarin. Exclusion Criteria: (i). Patient 1. Patient refusal, 2. Active mental illness or severe dementia, or being certified unfit to make medical decision by a specialist physician, 3. Pregnant Women (ii). Caregiver 1. Self-reported severe mental illness, dementia, active suicidal ideation, uncorrected hearing loss; 2. Unable to complete caregiver-reported outcomes.

Contact & Investigator

Central Contact

Xindi Huang, MSc Psychology

✉ huang.xindi@nccs.com.sg

📞 +65 63065636

Principal Investigator

Jolene Si Min Wong, MBBS, MMed (Surgery), MPH

PRINCIPAL INVESTIGATOR

Singapore General Hospital

Frequently Asked Questions

Who can join the NCT07789093 clinical trial?

This trial is open to participants of all sexes, aged 21 Years or older, up to 99 Years, studying Palliative Care. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07789093 currently recruiting?

Yes, NCT07789093 is actively recruiting participants. Contact the research team at huang.xindi@nccs.com.sg for enrollment information.

Where is the NCT07789093 trial being conducted?

This trial is being conducted at Singapore, Singapore.

Who is sponsoring the NCT07789093 clinical trial?

NCT07789093 is sponsored by Singapore General Hospital. The principal investigator is Jolene Si Min Wong, MBBS, MMed (Surgery), MPH at Singapore General Hospital. The trial plans to enroll 220 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology