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Understanding Quality of Life Among Patients With Cancer Receiving Palliative Care

Abramson Cancer Center at Penn Medicine logo

Abramson Cancer Center at Penn Medicine

Status

Active, not recruiting

Conditions

Cancer

Treatments

Behavioral: Offering Additional Resources to Promote Symptom Management

Study type

Interventional

Funder types

Other

Identifiers

NCT05331625
850807
UPCC 11922

Details and patient eligibility

About

This randomized controlled trial will assess the effects on quality of life of two approaches to symptom management among new patients referred to a palliative care oncology clinic.

Enrollment

208 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Be a new patient at an outpatient palliative care clinic
  • Resident of Pennsylvania
  • Over 18 years of age

Exclusion criteria

  • Prior use of certain symptom focused therapies
  • Currently pregnant

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

208 participants in 2 patient groups

Intervention
Experimental group
Description:
Participants in this group will consent to participate in a study about quality of life for patients with cancer seeking outpatient palliative care. They will be seen in a palliative care oncology clinic at which time they will be offered additional resources to promote symptom management. They will be asked to complete a series of surveys every two weeks for 16 weeks which will assess their quality of life, symptoms, and medication use.
Treatment:
Behavioral: Offering Additional Resources to Promote Symptom Management
Usual Care
No Intervention group
Description:
Participants in this group will consent to participate in a study about quality of life for patients with cancer seeking outpatient palliative care. They will be seen in a palliative care oncology clinic where they will receive symptom management and supportive care. They will be asked to complete a series of surveys every two weeks for 16 weeks which will assess their quality of life, symptoms, and medication use.

Trial contacts and locations

1

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Central trial contact

Nicholas S Bishop

Data sourced from clinicaltrials.gov

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