Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT03658083 |
Other study ID # |
228/16 |
Secondary ID |
|
Status |
Completed |
Phase |
|
First received |
|
Last updated |
|
Start date |
October 12, 2017 |
Est. completion date |
November 20, 2019 |
Study information
Verified date |
April 2022 |
Source |
Teesside University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
Background Surgery for lung cancer can be performed using open (thoracotomy) or minimally
invasive techniques (Video Assisted Thoracic Surgery (VATS)). Despite being associated with
fewer postoperative complications (PPCs) VATS is difficult to perform and is only used by
20-44% of thoracic surgeons in the UK. Robotic-Assisted Thoracic Surgery (RATS) maybe a more
attractive minimally invasive approach. To date, no studies have explored the impact of RATS
on exercise capacity or physical activity and although 1 study has looked at Heath Related
Quality of Life (HRQOL) post-RATS compared to an open technique indicators of surgical
technique were not controlled for. Furthermore, investigators have little understanding of
patients' experience of RATS.
Aims
1. To examine the variability of change in exercise capacity and health-related quality of
life (HRQOL) between those who receive thoracotomy V RATS.
2. To compare the difference in post-operative physical activity (step and activity count),
across 7 days, in those who receive thoracotomy V RATS.
3. To explore the manner in which patients appraise their experience of undergoing RATS.
Methods:
A mixed-method, multi-center study will be undertaken, utilizing a prospective
quasi-experimental study design and an interpretive phenomenological approach. 80
individuals, referred for a lung lobectomy with a primary or secondary diagnosis of lung
cancer, will complete outcomes assessed at 4 time-points. The Incremental Shuttle Walk Test
(ISWT) and the European Organization for Research and Treatment of Cancer Quality of Life
Questionnaire (EORTC QLQ C30) and the EORTC Lung Cancer module (EORTC QLQ LC13) will be
completed at: baseline, 3-6 days post surgery, 6-weeks post-surgery and at 3-month follow up.
Patients will wear an activity monitor immediately post-surgery until 1-week post-discharge.
Step and activity counts will be recorded. In-depth interviews will be conducted with up to
15 patients who underwent RATS to explore the manner in which patients appraise their
experience of RATS.
Description:
Lung cancer is the second most common cause of cancer in the UK and the most common cause of
cancer death. Surgery is currently the most effective treatment for curing lung cancer and it
can be performed using open (thoracotomy) or minimally invasive techniques (Video Assisted
Thoracic Surgery (VATS)). Despite VATS being associated with fewer postoperative
complications (PPCs), faster recovery and better survival at 4 years compared to thoracotomy
it is only used by 20-44% of thoracic surgeons in the UK and just 5% of surgeons in Europe
report using minimally invasive techniques for lung resection. Rigid, restrictive instruments
and suboptimal vision means a steep learning curve is necessary to conduct VATS successfully.
RATS maybe a more attractive minimally invasive approach as it offers 3DHD vision, a 360
degree view of the chest, and a fully articulated arm. JCUH and the Barts Hospital are two of
the few centers in the UK performing RATS.
Research on RATS has been largely limited to single retrospective case series reports
focusing on safety (PPCs and mortality) and cost effectiveness outcomes. Little research has
been conducted exploring the effect of RATS on patient-centered outcomes that are also
important quality measures.
To date, no studies have explored the impact of RATS on exercise capacity, yet investigators
know that individuals who undergo a thoracotomy have a 16% reduction in exercise capacity at
6 months follow up. Exercise capacity has been shown to be an important predictor for
long-term prognosis and length of stay following thoracic surgery, which can have substantial
implications for cost. Furthermore, percentage VO2 max has been shown to be the best
predictor of PPCs within 30 days of undergoing a lung resection (predictive value 85.5%),
which is an important indicator of patient safety.
Two studies have looked at HRQOL post-RATS and compared it to an open technique. Balduyck and
colleagues reported that whilst significant reductions from baseline were seen 1 month
post-surgery in those who underwent an open procedure (sternotomy), HRQOL had returned to
baseline values by 1 month post-surgery in those who underwent RATS. However, indicators of
whether individuals received RATS or an open procedure were not controlled for which is
likely to be important as individuals who have large tumors are not eligible to receive RATS.
Instead RATS is usually assigned to older, frailer individuals. The second study did conduct
between-groups comparisons between those who underwent a robotic lobectomy V those who
received an open rib and nerve sparing lobectomy. The mental-component of the SF-12 was
significantly higher in the robot group at 3 weeks post-surgery, indicating better mental
quality of life, although there were no significant between-group differences detected for
the physical-component. By 4 months follow up neither the mental nor the physical HRQOL
scores differed between the two groups. The SF-12 in a general measure of health status and
to date the impact of open surgery V RATS on disease-specific HRQOL has not been explored.
Physical activity is associated with improved HRQOL in patients with lung cancer and
increased survival post-diagnosis of cancer. However, 2 months following a lung resection,
performed via a thoracotomy or VATS, physical activity levels were still reduced.
Unfortunately comparisons between surgical groups were not possible in this study due to the
small number of patients who underwent VATS (14), therefore postoperative physical activity
in those who have undergone thoracotomy compared to minimally invasive surgery is still
unknown.
Clinical Commissioning Group (CCG) outcome indicator set 2015/16 includes enhancing quality
of life and ensuring patients have a positive experience of care (NHS England, 2015). To
date, no qualitative research exploring the patients' experience of RATS has been conducted
and investigators have little understanding of patients' experience of thoracic surgery in
general. Interestingly, a very recent study exploring preoperative nurses work experience
with robotics found that feelings of uncertainty and concerns about safety were common due to
a lack of education about the robot system. It is likely, these feelings of unease are
translated to patients during their preoperative consultation leading to heightened anxiety.
Furthermore, if nurses do not feel they have sufficient information about the robot system
they are unlikely to be educating patients fully about their procedure. A study exploring the
appraisals of patients' experience of RATS is important to identify ways in which both pre
and postoperative care can be improved.
It would seem literature is scare exploring the impact of RATS on outcomes that are likely to
be meaningful to patients. Therefore the overall aim of this study is to examine the impact
of RATS compared to thoracotomy on patient-centered outcomes and to explore the individuals'
experience of undergoing RATS.
Research strategy
Study design
A mixed-method, multi-center study will be undertaken, utilizing a prospective
quasi-experimental study design and an interpretive phenomenological approach.
Inclusion/exclusion criteria
Individuals referred for a lung resection with a primary or secondary diagnosis of lung
cancer will be eligible, although those with a tumor >7cm will be excluded. Individuals
referred for a lung resection via thoracotomy will be recruited from James Cook University
Hospital (JCUH), Middlesbrough and those referred for RATS will be recruited from JCUH or St
Bartholomew's hospital, London (Barts).
Recruitment
Once a referral for a lung resection via thoracotomy or RATS is received a cover letter and
information sheet, containing details of the study, will be mailed to patients along with
their clinic appointment letter. Interested patients will be encouraged to contact a member
of the research team, by telephone or email, to discuss the study in more detail. When
patients attend their preoperative clinic a member of the clinical team will request
permission for a member of the research team to approach them about participation in the
study. If individuals would like to participate in the study informed consent will be
obtained.
Surgical care
Prior to surgery all patients receive standard physiotherapy consisting of breathing
exercises and advice on activities postoperatively.
Three cardiothoracic surgeons, 2 at JCUH and 1 at Barts, will perform lung resections.
Consistent with usual care at JCUH and Barts all individuals will be transferred to sitting
at the bedside as soon as possible post-surgery and will be required to walk 150m before
being discharged home. At JCUH patients are also required to complete a flight of stairs and
cycle for five minutes (with no resistance).
Data collection
Demographic and anthropometric information will be collected at baseline at the preoperative
clinic visit including; age, sex, BMI, lung function (forced expiratory volume in one second
(FEV1) and forced vital capacity (FVC)), smoking history, comorbidities, cancer stage and
grade. Details of the operation (i.e. technique, time, surgeon, post-operative pain
management) will be documented. Length of stay, readmissions and PPCs will be recorded at 3
months follow-up. The same criteria will be used to define a PPC as applied by Brocki et al.
PPCs will be classified as minor (a score of 1), medium (a score of two) or severe (a score
of three). A PPC will be defined as clinically relevant if two or more items are graded as a
minor complication (score of 1) or one item is graded as a medium or severe complication
(scores ≥2).
Quantitative phase
Outcomes will be assessed at 4 time-points; at baseline in the preoperative clinic (1 day to
2 weeks prior to surgery), day 3 post-surgery, at the follow up postoperative clinic visit
(within 6 weeks post-surgery) and at an additional hospital visit which will take place at 3
months. The time taken to complete each assessment will be recorded, we estimate no more than
2 hours will be required to complete the outcome variables (ISWT, the European Organization
for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ C30) and the
EORTC Lung Cancer module (EORTC QLQ LC13)). Individuals will also be requested to wear an
activity monitor Actigraph G3TX (Actigraph) immediately post-surgery until 1-week
post-discharge. Data will be stored on the cardiothoracic database at JCUH or Barts and on an
IBM SPSS statistics database at Teesside University.
Qualitative phase
An interpretive phenomenological approach (IPA) will be applied to the collection and
analysis of the qualitative data. IPA aims to understand the lived experience of participants
in response to a specific event (i.e. undergoing surgery). Analysis examines in detail how an
event is experienced and what meaning is ascribed to that event.
An informal interview schedule consisting of open-ended questions will be developed in
conjunction with members of the cardiothoracic team. The questions will be developed to
stimulate narratives focusing on the experience of undergoing RATS whilst also permitting
other topics, important to the individuals, to be discussed.
In-depth interviews will be conducted on up to 15 patients who underwent RATS. The interviews
will be conducted at patient's homes one week following hospital discharge (at the same time
the activity monitor is collected). Interviews will be largely patient led, allowing
individuals to tell their own story in their own words and at their own pace.
Sample Size and Analysis Plan
Quantitative phase
The primary endpoint is exercise capacity measured by the ISWT (m) completed at patients'
6-week postoperative clinic. Based on the minimal clinically important difference (MCID)
(48m) for the ISWT (Singh et al 2008), the between-subjects variability in the measure, and
the variability in the change scores (the 7-week reliability). A conventional estimation with
90% power and 2 p=0.05 returned a required sample size of 80 patients, 40 per group. This is
based on an ANCOVA analysis model, where invetigators look at the differences in the change
in ISWT between groups, adjusted for any imbalance between groups in ISWT performance at
baseline
Qualitative phase
Analysis will involve conducting a close line-by-line analysis on each original transcript to
explore the claims and understandings of the participants. A second researcher will review
the original transcripts before the 'emerging themes' are agreed. Once agreed, 2 researchers
will transfer the 'emerging themes' across the entire data set, thereafter referring to them
as 'master themes' The final master themes will be presented to a third researcher and
agreed. Thematic mapping will be used to develop the relationship between themes. Finally,
the findings will be translated into a narrative account with verbatim extracts (quotes) to
provide a means of validation.