Exploring Physical and Psychological Needs and Quality of Life in Patients With Advanced Cancer Receiving Immunotherapy

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorTaipei Veterans General Hospital, Taiwan

About this trial

During the immune checkpoint inhibitor therapy (ICIT), most of the patients stay at home, but there is lacking of the studies to explore their physical and psychological distress, financial toxicity, care needs, and quality of life. Therefore, the aims of this program are to (1) explore the immune-related adverse event (irAE) severity, distress, financial toxicity, and quality of life and examine the psychometric testing of the Functional Assessment of Cancer Therapy-Immune Checkpoint Modulator (FACT-ICM); (2) establish the LINE group for assessing irAE severity and change trajectory of quality of life in one-year follow-up and (3) combined retrospective chart review and the finding in aim (2) to develop the risk prediction model in order to identify the high risk population.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

(1) Patients diagnose cancer and are informed

(2) Aged ≥18 years old

(3) Conscious clear and able to communicate

Disqualifiers

None

Trial population

Participants will be recruited at inpatients and outpatient clinic of department of chest medicine, department of oncology, division of gastroenterology and hepatology, and department of obsterics and gynecology.

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

200 Participants
are grouped into 2 trial groups
Group A: Aim 1: Cross-sectional study
Group B: Aim 2 and 3: Longitudinal follow-up

Trial outcomes

Primary outcomes

1

Patient-Report Outcome-- Common Terminology Criteria for adverse events (PRO-CTCAE)

Interviewers graded the severity of adverse events according to the Common Terminology Criteria for adverse events (CTCAE), version 5, from the National Cancer Institute (NCI). In this study, we included 33 important symptoms from PRO-CTCAE in immunotherapy patients.

Time frame
The data will be collected once a week within 3 months and once in 3-4 weeks in 4th-12th months during treatment.
2

Symptom Severity Scale (SSS)

The Symptom Severity Scale (SSS) was used to evaluate the symptom severity of cancer patients. It included 25 common symptoms in cancer patients.The severity was scored by an 11-point numerical rating scale, from 0 (not at all) to 10 (very severe).

Time frame
The data will be collected at five times (Before treatment for baseline, the 3rd, 6th, 9th, and 12th month)
3

Distress Thermometer (DT)

The Distress Theremometer is utilized to assess patients' emotional distress and its sources. The assessment was developed by National Comprehensive Cancer Network (NCCN) and to evaluate the psychological distress level of cancer patients. It a single-item-11-point scale, from 0 to 10 points, which ask patients about their overall distress level over the past week, with higher scores indicating higher levels of distress.

Time frame
The data will be collected at five times (Before treatment for baseline, the 3rd, 6th, 9th, and 12th month)
4

The COmprehensive Score for financial Toxicity-Functional Assessment of Chronic Illness Therapy (COST-FACIT)

The COST-FACIT developed by Souza, is used to assess patients' financial distress. It evaluates the financial situation of patients undergoing treatment for chronic diseases. The scale consists of 12 items rated on a 0 to 4 Likert-type scale, where 0 indicates "not at all important" and 4 indicates "very important." Lower scores indicate greater financial toxicity.

Time frame
The data will be collected at five times (Before treatment for baseline, the 3rd, 6th, 9th, and 12th month)

Secondary outcomes

Other outcomes

Sponsors and contacts

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Taipei Veterans General Hospital, Taiwan

Lead sponsor

National Yang Ming Chiao Tung University

Collaborator