NCT02263573

Brief Summary

The primary purpose of the protocol is to determine the effects of a new program of PEP'C "PEP'C with constant load and intermittent recovery" (PEP'C-R) on endurance parameters of older seniors. The study hypothesis: the investigators propose that PEP'C-R training offers a significant improvement in endurance parameters for older seniors. The secondary objectives are to determine the effects of PEP'C-R on maximal cardio-respiratory function, FMD (Flow-mediated dilation), PWV (pulse wave velocity), systolic and diastolic heart function, body composition (measured by impedance), biological, functional and cognitive functioning and quality of life.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
62

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Dec 2014

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 1, 2014

Completed
12 days until next milestone

First Posted

Study publicly available on registry

October 13, 2014

Completed
2 months until next milestone

Study Start

First participant enrolled

December 4, 2014

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 18, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 18, 2017

Completed
Last Updated

May 24, 2018

Status Verified

May 1, 2018

Enrollment Period

2.9 years

First QC Date

October 1, 2014

Last Update Submit

May 22, 2018

Conditions

Keywords

PEP'C-REndurance parametersMaximal cardio-respiratory functionOlder seniorsOver 70

Outcome Measures

Primary Outcomes (1)

  • Change in intensity in W of the first ventilatory threshold (VT1)

    Determine the intensity in W of the first ventilatory threshold (VT1) for the experimental group and for the control group.

    From baseline to 9.5 weeks

Study Arms (2)

PEP'C-R

EXPERIMENTAL

Subjects will benefit from one preliminary session and 18 sessions of PEP'C-R, (2 sessions per week for 9.5 weeks).

Other: PEP'C-R

Control group

ACTIVE COMPARATOR

Subjects do not participate in the program PEP'C-R and continue their usual activities at home for 9.5 weeks.

Other: Control group usual activities

Interventions

PEP'C-ROTHER

Preliminary session of calibration and tolerance: Test of Borg: determination of VT1 for 10 minutes, 3 min pedaling at 25 W and then 20 minutes pedaling on VT1 determined during the exercise test (ET) -10%. Session 1: 30 min of pedaling at constant load VT1 determined during exercise testing (EE) - 10%. Session 2 Session 17: increase in the burden of BASE (5 BASE \* 5 min: 25 min) by 10% and decrease in relation to the load of the PIC (5 PIC \* 1 min: 5 min) to get a cumulative charge of the same session. Changes in heart rate (HR) determine the evolution of sustained loads: a decrease of 10 bpm in heart rate leads to an increase by 10% in the intensity of the base (PIC load remains constant). Session 18 = Session 1.

PEP'C-R

Participants in the control group will not follow the intervention PEP'C-R. They will continue their usual activities for 9.5 weeks and will be assessed before and after this period. After the study, they will be offered the benefit of the conventional program of the PEP'C.

Control group

Eligibility Criteria

Age70 Years+
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)

You may qualify if:

  • Low physical activity determined using the questionnaire IPAQ in METs (\<3).
  • Informed about the results of examinations performed at screening visit.
  • Subject able to understand the purpose, procedures and risks of the study and give written informed consent.

You may not qualify if:

  • Contraindications to perform the cardiac stress test and PEP'C-R (Musculoskeletal limitations, Unstabilized heart Failure with chest pain on exertion under maximal medical therapy, ventricular and supraventricular disorders, Acute coronary syndrome within \<1 month, Unstabilized respiratory failure or oxygen-dependent)
  • Abnormality shown at the cardiac stress test : clinical abnormality (chest pain), electric abnormality (found on ECG), abnormal blood pressure, abnormality of the ventilatory system (bronchospasm, hypoxemia,...)
  • Cognitive impairment which exclude PEP'C-R training.
  • Current Cancer chemotherapy.
  • Visual Impairment which exclude PEP'C-R training.
  • Presence of fibromyalgia.
  • Subject treated with beta-blockers and other negative chronotropic molecules.
  • Dependent patient.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hôpitaux Universitaires de Strasbourg

Strasbourg, 67091, France

Location

Related Publications (1)

  • Bouaziz W, Schmitt E, Vogel T, Lefebvre F, Lepretre PM, Kaltenbach G, Geny B, Lang PO. Effects of a short-term Interval Aerobic Training Programme with active Recovery bouts (IATP-R) on cognitive and mental health, functional performance and quality of life: A randomised controlled trial in sedentary seniors. Int J Clin Pract. 2019 Jan;73(1):e13219. doi: 10.1111/ijcp.13219. Epub 2018 Jul 2.

Study Officials

  • Thomas VOGEL, MD, PhD

    CHRU Strasbourg

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 1, 2014

First Posted

October 13, 2014

Study Start

December 4, 2014

Primary Completion

October 18, 2017

Study Completion

October 18, 2017

Last Updated

May 24, 2018

Record last verified: 2018-05

Locations