Feasibility of a 8-week Telerehabilitation Program for Patients With Thoracic Neoplasia Receiving Chemotherapy

Lung Cancer Clinical Trial

— TELErp  

Official title:

Feasibility of an Eight-week Telerehabilitation Program for Patients With Unresectable Thoracic Neoplasia Receiving Chemotherapy

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02716493
• Other study ID #: 20994
• Status: Active, not recruiting
• Phase: N/A
• First received: March 10, 2016
• Last updated: January 5, 2017
• Start date: November 2013
• Est. completion date: July 2017

Study information

• Verified date: January 2017
• Source: Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec
• Contact: n/a
• Is FDA regulated: No
• Health authority: CANADA: Comité éthique CRIUCPQ
• Study type: Interventional

Clinical Trial Summary

Exercise-based rehabilitation improves physical function, fatigue and quality of life in patients with thoracic neoplasia. Consequently, the need for rehabilitation across the continuum of care in oncology is growing rapidly. However, the implementation of this type of intervention is limited because of many barriers such as patients' symptoms and poor accessibility to programs. In this context, healthcare systems should develop and implement new approaches to dispense these services. Consequently, telerehabilitation is a promising strategy to improve access and adherence to rehabilitation.

OBJECTIVES To investigate the feasibility, adherence and satisfaction of a home-based telerehabilitation program (TELERP) with real-time physiological parameters acquisition in patients with unresectable thoracic neoplasia receiving chemotherapy and to explore its effects on patients' functional capacity.

METHODS Five patients receiving chemotherapy followed an 8-week TELERP using real-time monitoring combined with interactive exercises. The TELERP included supervised (15) and unsupervised (9) strengthening and cardiovascular exercise sessions at a rate of 3 sessions/week. The feasibility of the TELERP, adverse outcomes, technical issues, program adherence and satisfaction were analysed. Prior to and after the program, a six-minute walking test (6MWT), a timed up and go (TUG) and a timed stair test (TST) were done to assess functional capacity

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 5
• Est. completion date: July 2017
• Est. primary completion date: July 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 80 Years

Eligibility

Inclusion Criteria:

• Patients had to have an ECOG functional status of 0 (Asymptomatic) or 1 (Symptomatic but completely ambulatory);

• Have a sufficient understanding of verbal and written French instructions

• Live in a geographic region served by a high speed Internet connection.

Exclusion Criteria:

• oxygen pulsed saturation (SpO2) <80% during the cardiopulmonary exercise test

• contraindications to exercise testing according to the American Thoracic Society and American College of Chest Physicians Exercise Testing Guidelines

• cerebral or bone metastasis

• a history of significant cardiovascular disease, hypertension, diabetes or musculoskeletal concerns that might limit their ability to perform active exercises

• severe psychiatric illness compromising adherence to the rehabilitation training routine.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label

Related Conditions & MeSH terms

• Lung Cancer

Intervention

Behavioral:
• Telerehabilitation program
The intervention was an 8-week home-based telerehabilitation program (three sessions of about 75 minutes per week) using the eChez-Soi telerehabilitation platform. Through a unique software interface, the eChez-Soi allows for the following three technological aspects: 1- continuous data acquisition and recording from commercial biometric sensors; 2- continuous transmission of the collected data via the Internet to the clinician's computer, allowing the clinician to visualize the biomechanical and physiological parameters in real time; and 3- a challenging gaming environment with interactive exercises performed on musical rhythms. In total, 15 supervised sessions and 9 unsupervised sessions were planned for a total of 24 exercise sessions

Locations

Country	Name	City	State
Canada	CRIUCPQ	Quebec

Sponsors (1)

Lead Sponsor	Collaborator
Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of adverse events during the 8-week telerehabilitation program		Along the 8-week program	Yes
Primary	Adherence of the participants to the 8-week telerehabilitation program.	Adherence was defined as the number of sessions done over the prescribed sessions (supervised and unsupervised) and as percentage of time spent within the target heart rate range (intensities) throughout the cardiovascular exercise sessions	Along the 8-week program	No
Primary	Participants satisfaction with the telerehabilitation platform with the Québec User Evaluation of Satisfaction with Assistive Technology questionnaire (QUEST 2.0)	The satisfaction of the patients was evaluated using a questionnaire adapted from the Québec User Evaluation of Satisfaction with Assistive Technology questionnaire (QUEST 2.0) that calculates both satisfaction scores for technological aspects and services. It consists of 12 items rated on a scale from 1 to 5 (1: not satisfied at all to 5: very satisfied).	At the end of the 8-week telerehabilitation program	No
Primary	User satisfaction with health services received with the French version of the Health Care Satisfaction Questionnaire	To assess more specifically the user satisfaction with health services received, we used the French version of the Health Care Satisfaction Questionnaire. This is a 26-item questionnaire answered on a four-point Likert scale, where ''1'' represents ''not at all satisfied'' and ''4'' represents ''highly satisfied". The total score is calculated in percentage and can be computed as the mean overall satisfaction divided in three domains: i) relationship with the professional, ii) delivery of services and iii) organization of services. Higher scores indicate a higher level of satisfaction.	At the end of the 8-week telerehabilitation program	No
Secondary	Cardiopulmonary maximal exercise test (CPET)		At baseline and following the 8-week program	No
Secondary	Constant workrate cycle exercise test at 80% of the maximal capacity of the patient		At baseline and following the 8-week program	No
Secondary	Isokinetic quadriceps muscle functions	Quadriceps muscle function (strength and endurance) was assessed during an isokinetic endurance test performed at a rate of 30 repetitions at 90°/sec of angular velocity (Biodex, system pro 4, Biodex Medical System, 20 Ramsay Road, Shirley, New York )	At baseline and following the 8-week program	No
Secondary	Lean body mass	Lean body mass (in Kg) were measured by bioelectrical impedance analysis (TBF-300WA Tanita, Arlington Heights, IL, USA)	At baseline and following the 8-week program	No
Secondary	Fat body mass	Fat body mass (in Kg) were measured by bioelectrical impedance analysis (TBF-300WA Tanita, Arlington Heights, IL, USA)	At baseline and following the 8-week program	No
Secondary	Weight	Weight (in Kg) of the patient	At baseline and following the 8-week program	No
Secondary	Height	Height (in meters) of the patient	At baseline and following the 8-week program	No
Secondary	Timed up and go test		At baseline and following the 8-week program	No
Secondary	Timed stairs test		At baseline and following the 8-week program	No
Secondary	Distance achieved during the 6 minutes walking test		At baseline and following the 8-week program	No
Secondary	Cancer specific quality of life with the self-reported European Organization for Research and Treatment of Cancer Quality of Life Questionnaire questionnaire	The cancer related quality of life was assessed using the self-reported European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-30) including the lung cancer specific questionnaire QLQ-LC13	At baseline and following the 8-week program	No
Secondary	Anxiety and depression with the Hospital Anxiety and Depression Scale questionnaire	The French Canadian version of the Hospital Anxiety and Depression Scale (HADS) was used to identify patients suffering of anxiety disorders or depression	At baseline and following the 8-week program	No
Secondary	Nutritional status with the mini-nutritional assessment		At baseline and following the 8-week program	No