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The Use of a Quality of Life Questionnaire in Patients With Lung Cancer

A Prospective Randomised Controlled Study to Investigate the Effectiveness of Using a Quality of Life Questionnaire to Target Interventions to Improve Quality of Life in Patients With Lung Cancer

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01213745
Enrollment
138
Registered
2010-10-04
Start date
2010-09-30
Completion date
2012-07-31
Last updated
2010-10-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Keywords

lung, cancer, quality of life

Brief summary

This study will investigate the effectiveness of using the European Organisation for Research and Treatment of cancer Core Quality of Life Questionnaire (EORTC QLQ-C30 + LC 13) to identify and target therapies in patients with lung cancer. The study will assess whether using the questionnaire will result in an improvement in QoL.

Detailed description

Patients with lung cancer who have completed a course of treatment (or who are in-between treatment) at the Royal Marsden Hospital would be eligible for inclusion in the study. Participants will be randomised into 3 groups. Group 1 - this group will complete the QoL questionnaire and will receive targeted therapies by a doctor (and other members of the oncology team) during a clinic consultation. Group 2 - will complete the QoL questionnaire however the questionnaire will not be seen by the doctor during a clinic consultation. Group 3 - the control group will not complete the QoL questionnaire before a clinic consultation. All patients will complete a diary of all contact they have with health care professionals during the study. The study will last for 6 weeks and at the end of the study all patients will complete the QoL questionnaire.

Interventions

OTHERIntervention
OTHERAttention
OTHERControl

Sponsors

Royal Marsden NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* male or female age \> 18 years * patients who are able to adequately understand written and spoken english * diagnosis of lung cancer (non small cell, small cell, mesothelioma) * no plan to commence treatment (chemotheraphy, targeted therapies, radioterhapy, surgery) with 6 weeks * both radically or palliatively treated patients remain eligible * patients whose toxicities from their primary treatment has resolved or have stabilised for a period of 7 days

Exclusion criteria

* patients are taking part on any other QoL studies * taking part in any other studies that requires QoL questionnaires, extra visits or investigations * currently on treatment (chemotherapy, radiotherapy, surgery or targeted therapies) * they have on going toxicities from their treatment which have not been stablised (required intervention within last 7 days)

Design outcomes

Primary

MeasureTime frame
To investigate whether the use of QOL questionnaires during the assessment and management of lung cancer patients results in improved quality of life

Secondary

MeasureTime frame
To investigate whether the use of EORTC QLQ-C30 + lung cancer module results in less patient contact with health care professionals during the 6 week study period for the 3 groups

Countries

United Kingdom

Contacts

Primary ContactDr M O'Brien
mary.o'brien@rmh.nhs.uk02086613278
Backup ContactMr M Laybourne
matthew.laybourne@rmh.nhs.uk02086613835

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026