Metabolic Flexibility and Autonomic Control After Muscle Power vs Metabolic Power Training in Postmenopausal Oncological Women: the POWER Health Study

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age35-75
SponsorUniversity of Valencia

About this trial

POWER Health is a randomized clinical trial with a two-arm parallel design whose objectives are 1) to study metabolic flexibility and autonomic function (both capacities that describe cardiovascular health) in a sample of postmenopausal oncological women vs postmenopausal untreated controls (CT); and 2) to analyze the impact of two different 8-week physical exercise supervised interventions: HIIT training vs strength training focused on muscle power, on both cardiovascular capacities in these populations.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients diagnosed of relapse free-cancer (RFC) or patients not diagnosed of any cancer at least the last 15 years (CG)

Aged between 35 and 75 years

Diagnostic of breast cancer (i.e., including ductal carcinoma, invasive carcinoma, triple negative; RFC) or physiological menopause (CG)

Not participating in a nutritional/dietary intervention

Disqualifiers

Medical contraindication for being engaged in an exercise.

Additional surgery planned within the intervention

Consuming usually betablocker or any drugs alterning nervous system functioning

History of another primary invasive cancer (RFC) or suffer a serious chronic illness (CG)

Trial design

Design model

Parallel

Treatments tested in this trial

  • HIIT program (8 weeks)

    Behavioral

    Metabolic Power Training: A High Intensity Interval Training (HIIT) intervention, 3 times per week (30 min session) during 8 weeks with professional supervision and intensities adapted and modified during the intervention period.

  • MPI program (8 weeks)

    Behavioral

    Muscle Power Intervention (MPI), 2 times per week (45 min session) during 8 weeks with professional supervision and intensities adapted and modified during the intervention period.

Treatment groups

56 Participants
are divided into 2 treatment groups
Group A: Exercise groupExperimental treatment 2 interventions
Group B: Control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Fat oxidation during incremental test

Fat oxidation rates calculated from VO2 and VCO2 values collected by indirect calorimetry (COSMED K5 portable metabolic analyzer, Rome, Italy) and after applying Frayn's stoichiometric formulae, during an incremental test from 0.45 W/kg with 0.15W/kg each 4-min step

Time frame
Preintervention (only this one in cross-sectional study) and Postintervention (8 weeks after)
2

Detrended Fluctuation Analysis

Non-linear mathematical variable that allows collecting physiological information and vagal activity of the organism, analysed in 2-minute intervals by Kubios Scientific software (Kuopio, Finland), during the incremental test

Time frame
Preintervention and Postintervention (8 weeks after)

Secondary outcomes

1

Weight

Weight measured with a scale (kg)

Time frame
Preintervention and Postintervention (8 weeks after)
2

Height

Height measured with a stadiometer (cm)

Time frame
Preintervention and Postintervention (8 weeks after)
3

Calf, waist and hip circumferences.

Calf, waist and hip circumferences will be assessed with an anthropometric tape measure (cm)

Time frame
Preintervention and Postintervention (8 weeks after)
4

Lean mass

Body composition assessment will be obtained by bioimpedance (Tanita DC-430 MA S; Tokyo, Japan; kg)

Time frame
Preintervention and Postintervention (8 weeks after)

Other outcomes

Sponsors and contacts

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University of Valencia

Lead sponsor

Generalitat Valenciana

Collaborator