VIrtual REality Glasses for the Enhancement of Acute BRACHYtherapy Tolerance for Endometrial Cancer Patients.

Endometrial Cancer Clinical Trial

— Vire-Brachy  

Official title:

VIrtual REality Glasses for the Enhancement of Acute BRACHYtherapy Tolerance for Endometrial Cancer Patients.

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03324958
• Other study ID #: 2017-0501
• Secondary ID: 2017-A01919-44
• Status: Terminated
• Phase: N/A
• Start date: March 26, 2019
• Est. completion date: March 4, 2021

Study information

• Verified date: February 2022
• Source: Centre Hospitalier Universitaire de Saint Etienne
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This randomized phase III multicenter trial aims to evaluate the impact of virtual reality helmets (visual and audio) during VCB in patients treated for endometrial cancer, in terms of pain and anxiety.

Description:

Endometrial cancer is one of the most common gynaecological cancers among women in the developed countries. After a curative surgical treatment, many relapses occur in the vaginal cuff. The PORTEC-2 trial has demonstrated a similar reduction in local relapses of intermediate- to high-risk endometrial cancer with vaginal cuff brachytherapy (VCB) than with external beam radiotherapy (EBRT). However, VCB induced less late toxicities. VCB is therefore indicated after surgery for intermediate- to high-risk endometrial cancer. VCB is also recommended after radiation therapy, for patients with stage II or III type 1 endometrial cancers according to the International Federation of Gynaecology and Obstetrics classification (FIGO), and for all patients with histological type 2 endometrial cancers.

If the late tolerance of VCB is correct, the acute tolerance remains limited, and is mainly characterized by local pain and anxiety) Virtual reality appears to be a promising tool to enhance treatment cancer tolerance, offering a safe and entertaining environment. By the way, the use of virtual reality could limit physical and psychical discomfort induced by VCB.

This randomized phase III multicenter trial aims to assess the impact of virtual reality helmets (visual and audio) during VCB in patients treated for endometrial cancer, in terms of pain (primary endpoint), and in terms of anxiety (secondary endpoint). Randomization will define which patient will wear a virtual reality helmet. Stratification will be performed according to the following criteria: vaginal molded applicator versus cylinder, two applications versus four; <70 years versus> 70 years.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 24
• Est. completion date: March 4, 2021
• Est. primary completion date: December 1, 2020
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients over 18 years old.

• Patients with endometrial cancer, with histological type I and II, regardless of the degree of differentiation.

• Patients with stage I, II or III endometrial cancer according to the FIGO classification.

• Patients treated with high-dose-rate vaginal cuff brachytherapy, with curative intent.

• Patients affiliated or entitled to a social security scheme.

• Patients who received information about the study and co-signed with the investigator the consent to participate at the study.

Exclusion Criteria:

• Patients with stage IV endometrial cancer according to FIGO classification.

• Patients presenting recurrence of endometrial cancer.

• Pregnant or nursing women.

• Patients under protection of justice or unable to give consent.

Related Conditions & MeSH terms

• Endometrial Cancer
• Endometrial Neoplasms

Intervention

Device:
• Virtual reality Helmet
The virtual reality helmet will be installed by a radiotherapist or a radiotherapy manipulator, just before the intra vaginal applicator. The virtual reality headset will be connected to a dedicated computer. The virtual reality program will run for 10 minutes which will cover the entire procedure for setting up the brachytherapy device. In order to optimize the distractive potential of virtual reality, four different virtual reality programs will be offered to patients during each brachytherapy fraction. These programs will be contemplative so as not to compromise the immobility of the patients during the installation of the brachytherapy applicator.

Other:
• No Virtual Reality Helmet
The radiotherapists can freely dialogue with the patients during the brachytherapy applicator' seating up, as in current practice.

Locations

Country	Name	City	State
France	Institut de Cancérologie Lucien Neuwirth	Saint-Priest-en-Jarez
France	Institut Gustave Roussy	Villejuif

Sponsors (4)

Lead Sponsor	Collaborator
Centre Hospitalier Universitaire de Saint Etienne	Centre Antoine Lacassagne, Gustave Roussy, Cancer Campus, Grand Paris, Institut de Cancérologie de la Loire

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mean pain during brachytherapy applicator installations	Pain assessment will be done with visual analogue scale pain (line of 10 centimeters without graduation : beginning of the line means no pain, and the terminal extremity means worst pain ever felt), before and after brachytherapy applicator setting up	1 week
Secondary	Pain during brachytherapy applicator installations, independently at each fraction	Pain assessment will be done with visual analogue scale pain (line of 10 centimeters without graduation : beginning of the line means no pain, and the terminal extremity means worst pain ever felt), before and after brachytherapy applicator setting up.	1 week
Secondary	Mean anxiety during brachytherapy applicator installations	Anxiety assessment will be done with visual analogue scale (line of 10 centimeters without graduation : beginning of the line means no pain, and the terminal extremity means worst pain ever felt) anxiety, before and after brachytherapy applicator setting up, and with Hamilton scale (scores will be comprised between 0 : no anxiety, and 30 : maximal anxiety) before brachytherapy applicator setting up.	1 week
Secondary	Quality of life, six to height weeks after brachytherapy	Quality of life assessment will be done with the the endometrial cancer (EC)-specific Quality of Life module of the European Organization for Research and Treatment of Cancer (EORTC QLQ-EN24).	6 to 8 weeks after brachytherapy
Secondary	Anxiety and depression, six to height weeks after brachytherapy	Anxiety and depression will be assessed six to height weeks after brachytherapy with the Hamilton Anxiety and Depression scale (scores will be comprised between 0 : no anxiety, and 30 : maximal anxiety).	6 to 8 weeks after brachytherapy
Secondary	Correlation between mean pain during brachytherapy applicator setting up and age	Correlation will potentially be established between pain during brachytherapy applicator setting up and age.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and G8 scale.	Correlation will potentially be established between pain during brachytherapy applicator setting up and G8 scale.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and histologic type of cancer.	Correlation will potentially be established between pain during brachytherapy applicator setting up and histologic type of cancer.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and FIGO stage.	Correlation will potentially be established between pain during brachytherapy applicator setting up and FIGO stage.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and Performance status.	Correlation will potentially be established between pain during brachytherapy applicator setting up and Performance status.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and patient weight.	Correlation will potentially be established between pain during brachytherapy applicator setting up and patient weight.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and marital status.	Correlation will potentially be established between pain during brachytherapy applicator setting up and marital status.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and socio educational status	Correlation will potentially be established between pain during brachytherapy applicator setting up and socio educational status.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and number of pregnancies.	Correlation will potentially be established between pain during brachytherapy applicator setting up and number of pregnancies.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and history of pelvic surgery	Correlation will potentially be established between pain during brachytherapy applicator setting up and history of pelvic surgery.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and the number of concomitant treatment.	Correlation will potentially be established between pain during brachytherapy applicator setting up and the number of concomitant treatment.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and the nature of concomitant treatment.	Correlation will potentially be established between pain during brachytherapy applicator setting up and the nature of concomitant treatment.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and the nature of cancer treatments	Correlation will potentially be established between pain during brachytherapy applicator setting up and the nature of cancer treatments.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and the supportive cares performed	Correlation will potentially be established between pain during brachytherapy applicator setting up and the supportive cares performed.	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and the radiotherapy scheme	Correlation will potentially be established between pain during brachytherapy applicator setting up and the radiotherapy achievement	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and the brachytherapy scheme	Correlation will potentially be established between pain during brachytherapy applicator setting up and the brachytherapy scheme	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and the radiotherapy induced toxicities (describe according to the Common Terminology Criteria for Adverse Events 4.4)	Correlation will potentially be established between pain during brachytherapy applicator setting up and the radiotherapy induced toxicities (describe according to the Common Terminology Criteria for Adverse Events 4.4).	1 week
Secondary	Correlation between mean pain during brachytherapy applicator setting up and the toxicities of previous brachytherapy fractions (describe according to the Common Terminology Criteria for Adverse Events 4.4).	Correlation will potentially be established between pain during brachytherapy applicator setting up and the brachytherapy induced toxicities (describe according to the Common Terminology Criteria for Adverse Events 4.4).	1 week