ClinicalTrials.Veeva

Menu

Descriptors and Predictors of Burden and Information Needs

C

Chulabhorn Cancer Center

Status

Completed

Conditions

Advanced Lung Cancer
Symptoms

Treatments

Other: questionnaires

Study type

Observational

Funder types

Other

Identifiers

NCT04069494
200180015

Details and patient eligibility

About

the purpose of this study is to investigate over time patients' symptom burden, caregiving burden, and patients and caregivers' need for information on patient symptom self-management at home during palliative radiotherapy(RT) for lung cancer. Repeatedly assessing burden and information needs on symptom self-management at home can help healthcare professionals to design a bespoke service and plan of care for both patients and family caregivers. In addition, I will explore psycho-social and clinical predictors of burden and information needs in patients and caregivers. These predictors can help health professionals to identify patients and caregivers at risk for distress during palliative radiotherapy for lung cancer.

Full description

Eligible patients will be invited to take part in the study via a patient information sheet. They will also be asked to nominate their primary caregiver, who will also be invited to take part in the study. We will give patients and caregivers 24 hours to decide whether they want to take part or not. If they do decide to take part, all research participants will be involved in the study on four consecutive occasions before, during and after their treatment. These four time points will be the following:

  • before first fraction of RT
  • 1st week of RT (1st-5th faction)
  • 2nd week of RT (6th-10th fraction)
  • 1 month after the last fraction of RT The principal researcher, i.e. Saengrawee Thanthong, will endeavour to collect questionnaires in the hospital. If participants cannot come to the hospital to receive radiotherapy or for their follow up appointment and complete the questionnaire, then the principal researcher will call them and offer to complete the questionnaires over the phone so as to minimise missing data due to attrition.

Enrollment

112 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:• Inclusion criteria for patients:

  • Histological diagnosis of Lung cancer with stage III-IV(TNM)

  • Age: 18 years or over

  • Planning for palliative RT

  • Scheduled to receive up to 10 fractions of palliative radiotherapy (Stevens, Macbeth, Toy, Coles, & Lester, 2015)

    • Exclusion criteria for patients:

  • Non-English, Non-Thai speaking

  • Diagnosis of severe cognitive or mental illness that affects communication

Patients' family caregivers will also be invited to participate as per below:

  • Inclusion criteria for caregivers:

    • Family member of the care recipient can be spouse, child, parent, friend etc.
    • Age: 18 years or over
    • Only one family member if the patient presents with more than one.
    • Same person in every time point
  • Exclusion criteria for caregivers:

    • Non-English, Non-Thai speaking

Trial design

112 participants in 2 patient groups

patients
Description:
People diagnosed with advanced lung cancer and scheduled to receive palliative RT will be invited to participate between 1st July 2019 and 31st January 2020.
Treatment:
Other: questionnaires
care giver
Description:
Patients' family caregivers will also be invited to participate
Treatment:
Other: questionnaires

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems