Assessment and Modulation of Energy Balance in Cachectic Patients Using Adapted Physical Activity

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorUniversity of Rennes 2

About this trial

1. OBJECTIVE OF THE STUDY The study consists of evaluating resting energy expenditure (REE) and that induced by adapted physical activity (APA) in cachectic patients, compared with those predicted by equations and those of non-cachectic cancer patients. We will also seek to identify potential compensations in the level of Physical Activity (PA) and dietary intake during one week of the PA programme. 2. CONDUCT OF THE STUDY Taking part in this study will in no way affect your treatment at SPORMED; you will undergo the same assessments and carry out the PAA programme in the same way. As a reminder, your treatment at SPORMED consists of an initial assessment session, a 12-week ABS programme and a final assessment session.

If you take part in the EMC2APA study, we will ask you to measure your gas exchange at rest (60 minutes) and during the aerobic part of one of your physical activity sessions. You will perform the effort traditionally targeted during the sessions (constant moderate intensity (60% of your Reserve Heart Rate, equivalent to a perception of the difficulty of the effort of 5-6/10) while your gas exchanges will be measured using a portable, non-invasive measuring device (K5, COSMED®). You will also be fitted with an accelerometric wristwatch.

In addition to the gas exchange measurements that will take place in the SPORMED structure, we will ask you to fill in a logbook tracking your daily physical activity and your daily food intake. You will also be asked to wear an accelerometer in a belt attached to your hip for 7 days.

Participation in this study is voluntary. There are no restrictions during the protocol.

Eligibility criteria

Qualifiers

Be at least 18 years old.

Have understood the objectives of the study.

Have read and signed the consent form.

Be affiliated with a social security system.

Disqualifiers

Une fatigue extrême

Une anémie symptomatique (hémoglobine ≤ 8 g/dl)

Un syndrome infectieux sévère en cours d'évolution

Une décompensation de pathologie cardio-pulmonaire

Trial design

Treatments tested in this trial

  • Measuring energy balance

Treatment groups

10 Participants
are divided into 1 treatment group

Sponsors and collaborators