Optimal Timing of Physical Activity in Cancer Treatment

Metabolic Syndrome Clinical Trial

— ACT  

Official title:

Optimal Timing of a Tailored Physical Activity Program During Chemotherapeutic Cancer Treatment to Reduce Long-term Cardiovascular Morbidity

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01642680
• Other study ID #: 2012-0010
• Secondary ID: 41087
• Status: Completed
• Phase: N/A
• Start date: January 24, 2013
• Est. completion date: October 22, 2020

Study information

• Verified date: May 2024
• Source: University Medical Center Groningen
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The number of long-term cancer survivors is growing. As a result, treatment-related morbidity - such as cardiovascular disease, metabolic syndrome, functional decline and fatigue - is impacting quality of life and impairing survival. Metabolic syndrome in the general population is currently treated with lifestyle advice to increase physical activity (PA) and reduce caloric intake. This approach is still underused as standard care for cancer survivors. The aim of this study is investigate whether a tailored PA program that starts early (during curative chemotherapy with cardiovascular toxic potential) is superior in terms of reducing long-term cancer-treatment-related metabolic syndrome and cardiovascular morbidity to a program that starts late (after completion of chemotherapy).

Description:

Improved treatment is partly responsible for the increased survival and life expectancy in cancer patients. However, such treatment can be harmful as well, and cancer survivors therefore, face an increased risk of second malignancies and other chronic diseases, e.g. cardiovascular diseases and metabolic syndrome.

Due to the growing number of cancer patients and survivors, attention for rehabilitation, especially physical training, is growing. Several meta-analyses show the beneficial effects of physical training on several outcomes such as physical fitness, muscle strength, fatigue and quality of life, and a few studies showed the effect of exercise on physical active behaviour. However, studies on the effect of timing of exercise are lacking.

The present study aims to insert a tailored physical activity program early versus late in the chemotherapy based cancer treatment and will yield data about its safety and efficacy. We hypothesize that a tailored physical activity program during early cancer treatment may more be effective to reduce long-term cancer treatment toxicities and morbidity in cancer survivors compared to a program after cancer treatment.

Primary Objective: To investigate whether a tailored physical activity program that starts during chemotherapy (early) is superior in terms of physical fitness, as determined by VO2 peak at one year, to a program that starts after completion of chemotherapy (late).

Secondary Objectives: To examine the effect of the physical activity program on muscle strength and activity level, change in metabolic and cardiovascular damage parameters, cardiovascular risk factors and quality of life including self-efficacy, motivation for exercise, and fatigue.

Design: This protocol describes a multicenter, randomized study with 2 arms. Patients who will be treated with curative systemic chemotherapeutic treatment for testicular cancer, early colon cancer, early breast cancer or B-NHL will be randomized into an early or late PA program group. The early group will start the PA program during chemotherapy (for 12 weeks) until 12 weeks after completion of chemotherapy (total 24 weeks of training). The late group will start the same program (total of 12 weeks) after completion of chemotherapy. The longitudinal effects of the physical activity (PA) program for all participants will be evaluated at different time points in the UMCG: before start of chemotherapeutic treatment; at the start of the PA program and at 3, 6, 18 months after starting the PA program and 18 months after the last chemotherapy.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 266
• Est. completion date: October 22, 2020
• Est. primary completion date: October 22, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Patients with testicular, early colon, breast cancer or B-NHL with an indication for systemic chemotherapy with a curative intent

• Normal blood count at start of systemic treatment

• Patients need to have an adequate physical health, which is defined by diastolic blood pressure >45 mm Hg or <95 mm Hg; heart frequency in at rest < 100 per minute; body temperature below 38°C; respiration frequency in rest below 20 per minute

• Adequate cardiac function with a LVEF above the lower limit of normal

• Written informed consent

Exclusion Criteria:

• Infections requiring actual antibiotics

• Signs of ongoing bleeding or fresh petechiae; unexplained bruises

• Critical organ impairment due to their malignancy

• Not recovered from earlier surgical intervention

• Non adequate control of any symptoms of the malignancy

• Inability to travel independently to the rehabilitation centre

• Cognitive disorder or emotional instability that might impede the participation in the training program

• Recent cardiovascular event

Related Conditions & MeSH terms

• Cardiovascular Risk Factors
• Fatigue
• Metabolic Syndrome
• Vascular Diseases
• Vascular Disorders

Intervention

Other:
• A tailored physical activity program during chemotherapy
The early group will start the PA program during chemotherapy for 3 months, and after completion of chemotherapy for 3 months (total 6 months). The PA program will consist of two components: improvement of physical fitness and empowerment to adopt a healthy lifestyle. Longitudinal effects of this PA program will be evaluated at 5 time points: before chemotherapy; at start of the PA program and at 3, 6 and 18 months after start of the PA program. Safety parameters will be monitored throughout the study period.
• A tailored physical activity program after chemotherapy
The late group will start the PA program after completion of the chemotherapy for 6 months. The PA program will consist of two components: improvement of physical fitness and empowerment to adopt a healthy lifestyle. Longitudinal effects of this PA program will be evaluated at 5 time points: before chemotherapy; at start of the PA program and at 3, 6 and 18 months after start of the PA program. Safety parameters will be monitored throughout the study period.

Locations

Country	Name	City	State
Netherlands	University Medical Centre Groningen	Groningen

Sponsors (1)

Lead Sponsor	Collaborator
University Medical Center Groningen

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Difference in VO2 peak between the groups after completion of the PA program, measured by cardiopulmonary exercise testing (CPET).	The aim of this study is investigate whether a tailored PA program that starts early (during curative chemotherapy with cardiovascular toxic potential) is superior in terms of reducing long-term cancer-treatment-related metabolic syndrome and cardiovascular morbidity to a program that starts late (after completion of chemotherapy).; The VO2 at the peak of the exercise will be defined as peak oxygen uptake (VO2 peak), measured by cardiopulmonary exercise testing (CPET) on a stationary bicycle ergometer. The CPET is considered to be the most precise measure of cardio-respiratory fitness and is recommended for use in order to determine a patient's objective or subjective difference in exercise capacity	1,5 year
Secondary	Muscle strength using a hand-held dynamometer	Maximal voluntary isometric muscle force of the right and left extremity of extension of the knee, flexion of the knee, flexion of the elbow and extension of the elbow will be measured using a hand-held dynamometer. The "break method" will be used for all measurements. To employ this technique, the examiner gradually overcomes the force exerted by the patient until the extremity gives way. All measurements will be performed at least three times, with recovery intervals of at least 10 seconds. The peak forces (in Newtons) will be recorded and mean values of three technically correct measurements will be taken for analysis.	1,5 year
Secondary	Intima media thickness will be measured with vascular ultrasound	Vascular damage will be determined with the intima-media thickness (IMT) of the common carotid artery and femoral artery, performed with an Ultrasound technique.	1,5 year
Secondary	Cholesterol levels, measured in blood	Measured in blood, in mmol/L	1,5 year
Secondary	Triglyceride levels, measured in blood	Measured in blood, in mmol/L	1,5 year
Secondary	Glucose levels, measured in blood	Measured in blood, in mmol/L	1,5 year
Secondary	Body mass index, calculated with formula (see below)	BMI (body mass index): weight in kilograms divided by height in meters squared	1,5 year
Secondary	Health related quality of life measured with the EORTC QLQ-C30	Quality of life will be measured with the European Organization for Research and Treatment of Cancer (EORTC), Quality of Life Questionnaire Core 30 (QLQ-C30) version 3.0 questionnaire	1,5 year
Secondary	Patient reported self-efficacy measured using the ALCOS instrument	Patient reported general self-efficacy, measuring the patients' expectations of their general capacities, will be evaluated using the Dutch version of the General Self-Efficacy Scale (GSES), the "Algemene Competentie Schaal" (ALCOS)	1 year
Secondary	Patient reported fatigue measured with the Multi-dimensional Fatigue Inventory	The Multi-dimensional Fatigue Inventory is a validated 20-item questionnaire on different domains of fatigue	1,5 year
Secondary	Patient reported physical activity level with the PASE questionnaire	Physical activity will be assessed with the Sum score of the Physical Activity Scale for the Elderly questionnaire (PASE). This questionnaire consists of questions on leisure time, household and work-related activities.	1,5 year
Secondary	DNA collection	Whole blood will be drawn of patients and collected in EDTA tubes. DNA isolations and the Global Screening Array will be performed at the Human Genomics Facility (HuGeF) of the Genetic Laboratory of the Department of Internal Medicine at Erasmus MC, Rotterdam, the Netherlands	1,5 year
Secondary	Diffusion capacity of the lungs	Corrected for hemoglobin.	1,5 year
Secondary	Forced vital capacity (FVC) will be assessed by use of dynamic spirometry	Measured by means of dynamic spirometry	1,5 year
Secondary	Forced expiratory volume in one second (FEV1) will be assessed by use of dynamic spirometry,	Measured by means of dynamic spirometry	1,5 year
Secondary	FEV1/FVC ratio will be assessed by use of dynamic spirometry,	Measured by means of dynamic spirometry	1,5 year
Secondary	Senescence with markers of the senescence- associated secretory phenotype	Senescence will be measured in a subset of testicular cancer patients.; Markers of scenescence will be obtained from a skin biopsy and fat biopsy. Also, additional blood samples will be assessed to establish markers of the senescence- associated secretory phenotype.	1,5 year
Secondary	Cardiac function with echocardiography (Ultrasound technique)	Cardiac function will be measured at baseline and at the final measurement (e.g. left ventricular ejection fraction)	1,5 year
Secondary	Body composition will be assessed with a DEXA scan	With the DEXA scan, measurements of body composition will be obtained.	1,5 year
Secondary	PAI-antigen, measured in blood serum	Endothelial activation will be determined with PAI antigen in blood serum, in ug/L	1,5 year
Secondary	t-PA, measured in blood serum	Endothelial activation will be determined with t-PA antigen in blood serum, in ug/L	1,5 year
Secondary	Factor VIII, measured in blood serum	Endothelial activation will be determined with factor VIII in blood serum, in %	1,5 year
Secondary	Von Willebrand factor, measured in blood serum	Endothelial activation will be determined with von Willebrand facor in blood serum, in %	1,5 year
Secondary	Fibrinogen, measured in blood serum	Endothelial activation will be determined with fibrinogen in blood serum, in g/L	1,5 year
Secondary	Advanced glycation end products (AGEs) will be determined by measuring skin auto fluorescence.	Advanced glycation end products will be measured with an AGEreader	1,5 year
Secondary	Blood pressure, measured with a blood pressure cuff	Systolic and diastolic blood pressure in mmHg	1,5 years
Secondary	Fat percentage with skinfold measurement	Skinfold measurement of biceps, triceps, sub scapula and supra iliaca	1.5 years