Recruiting

Observational Study

Sponsor:

Dartmouth-Hitchcock Medical Center

Code:

NCT07195513

Conditions

Palliative Care Referral

Advanced Cancer

Palliative Care, Health Services

Metastatic Cancer (Different Solid Tumour Types)

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

ePRO-Directed Referral and Navigation to Palliative/Supportive Care

ePRO Symptom Monitoring with Usual Palliative Care Referral

Study Details

Brief summary:

This study is testing whether electronic surveys can help patients with advanced cancer report their symptoms and care needs so their doctors can connect them to palliative/supportive care services sooner. The goal is to see if this approach can make it easier for patients to get support for symptoms, quality of life, and other needs during cancer treatment.

Conditions

Palliative Care Referral

Advanced Cancer

Palliative Care, Health Services

Metastatic Cancer (Different Solid Tumour Types)

Study ID

NCT07195513

Start date

Feb 25, 2026

Status verified date

Mar, 2026

Completion date

Dec, 2028

Anticipated

Primary completion date

Apr, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria

1. Age ≥18 years.
2. Diagnosis of unresectable or metastatic, incurable thoracic, gastrointestinal, or breast solid tumor.
3. Receiving active cancer-directed therapy longitudinally in the outpatient oncology clinic and expected to continue treatment.

Exclusion Criteria

1. Members of vulnerable populations, including infants, minors, individuals unable to provide informed consent, and those who are incarcerated or imprisoned at the time of enrollment.
2. Already established with palliative care, defined as having a scheduled future palliative care appointment, a pending referral, or a visit with palliative care within the past 90 days.
3. Unable to provide informed consent in English.
4. Cognitive impairment that, in the judgment of the treating clinician, would preclude study participation.

Study Design

Enrollment

90 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Supportive Care

Interventions and Outcome Measures

Arms

experimental: ePRO-Directed Referral Intervention

Participants receive: (1) palliative care education from a trained study coordinator; (2) weekly electronic patient-reported outcome (ePRO) symptom monitoring surveys; (3) monthly ePRO palliative care surveys; and (4) navigation to palliative care services when a referral is placed. Severe or persistent patient-reported symptoms or unmet care needs identified through ePROs will trigger an alert to the oncology team with a recommendation for palliative care referral.

other: ePRO Symptom Monitoring with Usual Palliative Care Referral

Participants will be offered weekly electronic patient-reported outcome (ePRO) symptom monitoring surveys and instructions on contacting the oncology team for symptom management. Referral to palliative care occurs according to usual clinical practice. Current standard of care processes for managing symptoms at DCC vary across clinics and may or may not include ePRO monitoring based on the practice of the individual clinician and disease team.

Interventions

ePRO-Directed Referral and Navigation to Palliative/Supportive Care

This intervention combines routine electronic patient-reported outcome (ePRO) symptom monitoring with additional components designed to connect patients more directly to palliative/supportive care. In addition to weekly ePRO symptom surveys, participants complete a monthly palliative care-focused ePRO survey, receive structured palliative care education from a trained study coordinator, and are offered navigation support to facilitate access to palliative/supportive care services. Severe or persistent symptoms or unmet needs reported on ePROs generate an alert to the oncology team along with a recommendation for palliative care referral. This multicomponent approach is intended to address gaps in timely referral and access to palliative/supportive care that are not addressed through symptom monitoring alone.

ePRO Symptom Monitoring with Usual Palliative Care Referral

Participants will be offered weekly electronic patient-reported outcome (ePRO) symptom monitoring surveys and instructions on contacting the oncology team for symptom management. Referral to palliative care occurs according to usual clinical practice. Current standard of care processes for managing symptoms at DCC vary across clinics and may or may not include ePRO monitoring based on the practice of the individual clinician and disease team. Unlike the intervention arm, participants do not receive structured palliative care education, a monthly palliative care-focused ePRO survey, navigation support, or referral alerts generated from persistent or severe symptoms and unmet care needs.

Primary outcome measure

  • Feasibility of the Intervention & Trial Methods [ Time Frame: 12 and 24 weeks ]

Central Contacts and Locations

Central contacts

Locations

Dartmouth-Hitchcock Medical Center

Recruiting

Lebanon, New Hampshire, United States, 03756

Contacts

More Information

Sponsor

Dartmouth-Hitchcock Medical Center

Last update posted

Mar 10, 2026

Last verified

Mar, 2026

Keywords

  • ePROs
  • Patient Reported Outcomes
  • Palliative Care
  • Supportive Care
  • Advanced Cancer
  • Metastatic Cancer

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Dartmouth-Hitchcock Medical Center on 2026-03-10.