Suspended

Quality of Life in Cancer Patients Receiving Palliative Care

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
Study Aim

The study aims to evaluate how palliative care affects the quality of life in cancer patients using a detailed questionnaire.

What is being tested

Offering Additional Resources to Promote Symptom Management

Behavioral
Who is being recruted

Neoplasms

Over 18 Years
See all eligibility criteria
How is the trial designed

Supportive Care Study

Interventional
Study Start: November 2022
See protocol details

Summary

Principal SponsorAbramson Cancer Center at Penn Medicine
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: November 3, 2022

Actual date on which the first participant was enrolled.

This study focuses on understanding how different ways of managing symptoms can affect the quality of life for cancer patients who are receiving palliative care. Palliative care is a type of care that helps to improve the comfort and quality of life for people with serious illnesses. The trial aims to compare two different methods of symptom management to see which one better supports patients' overall well-being. This research is important because it seeks to find more effective ways to improve the day-to-day lives of patients dealing with serious health challenges. Participants in the study will be randomly assigned to one of the two symptom management approaches. The effectiveness of these approaches will be evaluated through a questionnaire called the McGill Quality of Life Questionnaire Revised (MQOL-R), which consists of 15 questions designed to assess both general and specific aspects of a person's quality of life. The study does not involve any physical interventions like medications or surgery, focusing instead on evaluating how different care approaches impact the patient's experience. By measuring quality of life in this way, the study aims to identify the best strategies to support patients' comfort and well-being.

Official TitleUnderstanding Quality of Life Among Patients With Cancer Receiving Palliative Care
NCT05331625
Principal SponsorAbramson Cancer Center at Penn Medicine
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

208 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Supportive Care Study

These studies explore ways to improve comfort and daily life for people living with a condition. They may focus on easing symptoms, reducing treatment side effects, or supporting overall well-being.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Neoplasms

Criteria

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

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
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.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

University of Pennsylvania

Philadelphia, United StatesOpen University of Pennsylvania in Google Maps
SuspendedOne Study Center