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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05696990
Other study ID # P2020/489
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2019
Est. completion date August 30, 2023

Study information

Verified date February 2024
Source Université Libre de Bruxelles
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aim of the clinical monocentric study is to assess the resistance training exercise intervention in patients with Heart Failure with reduced Ejection Fraction (HFrEF) and coronary artery disease that will best improve peak oxygen uptake (Peak Vo2) and leg strength (assessed Isokinetic). The investigators hypothesize that resistance training exercise with induced a high stress metabolic is more important exercise with induced than a lower stress metabolic.


Recruitment information / eligibility

Status Completed
Enrollment 112
Est. completion date August 30, 2023
Est. primary completion date March 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Clinical Coronary artery diseases - Heart failure with reduced ejection fraction Exclusion Criteria: - angina - acutely decompensated heart failure - electrocardiographic evidence of ischemia - significant valvular disease - orthopedic/neurologic disorders that limited exercise

Study Design


Intervention

Other:
3/7 Resistance Training Method
3/7 Resistance Training Method
3X9 Resistance Training Method
3X9 Resistance Training Method

Locations

Country Name City State
Belgium Erasme Hospital Brussels

Sponsors (1)

Lead Sponsor Collaborator
Université Libre de Bruxelles

Country where clinical trial is conducted

Belgium, 

References & Publications (2)

Duchateau J, Stragier S, Baudry S, Carpentier A. Strength Training: In Search of Optimal Strategies to Maximize Neuromuscular Performance. Exerc Sport Sci Rev. 2021 Jan;49(1):2-14. doi: 10.1249/JES.0000000000000234. — View Citation

Stragier S, Baudry S, Carpentier A, Duchateau J. Efficacy of a new strength training design: the 3/7 method. Eur J Appl Physiol. 2019 May;119(5):1093-1104. doi: 10.1007/s00421-019-04099-5. Epub 2019 Feb 12. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Peak VO2 after 3 months Change in Peak oxygen consumption (VO2) after three 3 months intervention Baseline and 3 months
Primary Change in strength knee extensor after 3 months Change in strength knee extensor (60°/sec) after three months intervention Baseline and 3 months
Secondary Change in VE/VCO2 slope after 3 months Change in ventilatory efficiency (VE/VCO2) slope at baseline and 3 months intervention Baseline and 3 months
Secondary Change in submaximal exercise capacity after 3 months Submaximal exercise capacity will be measured using watts at the first ventilatory threshold (VT1) Baseline and 3 months
Secondary Change in workload maximal after 3 months Change in workload max at baseline and 3 months intervention Baseline and 3 months
Secondary Change in Body fat after 3 months Change in Body fat at baseline and 3 months intervention Baseline and 3 months
Secondary Change in lean mass after 3 months Change in lean mass at baseline and 3 months intervention Baseline and 3 months
Secondary Change in leg lean mass after 3 months Change in leg lean mass at baseline and 3 months intervention Baseline and 3 months
Secondary Change in bone mass after 3 months Change in bone mass at baseline and 3 months intervention Baseline and 3 months
Secondary Change in Visceral adipose tissue after 3 months Change in Visceral adipose tissue measure by Dual-energy X- ray absorptiometry (DEXA) at baseline and 3 months intervention Baseline and 3 months
Secondary Change in hand grip force after 3 months Change in hand grip force on non dominant hand at baseline and 3 months intervention Baseline and 3 months
Secondary Change in ventilation metaboreflex function after 3 months Change in ventilation during metaboreflex test at baseline and 3 months intervention (Briefly, the subject is asked to exercise with the non-dominant arm by performing two 5 min handgrip manoeu- vres reaching approximately 50% of pre-determined maximal con- traction, in random order, separated by a 30 min interval: one bout with circulatory occlusion during the last 10 s of exercise and the all 3 min recovery phase ('clamp session'). During the clamp session, forearm cuff inflation to 30 mmHg above systolic blood pressure from the last 10 s of exercise till the end of the 3 min recovery phase; after cuff inflation, the subject is instructed to relax. Ergore- ceptor sensitivity is quantified as the percentage of the ventilatory and haemodynamic response to exercise maintained by circulatory occlusion during the third minute compared with the third minute of basal recovery.) Baseline and 3 months
Secondary Change in diastolic blood pressure metaboreflex function after 3 months Change in diastolic blood pressure during metaboreflex test at baseline and 3 months intervention Baseline and 3 months
Secondary Change in heart rate at rest after 3 months Change in heart rate at baseline and 3 months intervention Baseline and 3 months
Secondary Change in resting heart rate variability at rest after 3 months Change in resting heart rate variability at baseline and 3 months intervention Baseline and 3 months
Secondary Change 30 s sit-to-stand after 3 months Change 30 s sit-to-stand at baseline and 3 months intervention Baseline and 3 months
Secondary Change in isometric strength knee extensor after 3 months Change in strength knee extensor (isometric) at baseline and 3 months intervention Baseline and 3 months
Secondary Change in 120°/sec strength knee extensor after 3 months Change in strength knee extensor (120°/sec) at baseline and 3 months intervention Baseline and 3 months
Secondary Change in 180°/sec strength knee extensor after 3 months Change in strength knee extensor (180°/sec) at baseline and 3 months intervention Baseline and 3 months
Secondary Change strength knee extensor in leg extension after 3 months Change in one repetition maximal in leg extensor machine at baseline and 3 months intervention Baseline and 3 months
Secondary Change in sub maximal strength knee extensor in leg extension after 3 months Change in 10 repetitions maximal in leg extensor machine at baseline and 3 months intervention Baseline and 3 months
Secondary Change in heart rate recovery after 3 months Change in heart rate recovery at baseline and 3 months intervention Baseline and 3 months
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