High-Intensity Interval Training for Older Adults
- Conditions
- Age-Related Sarcopenia
- Interventions
- Other: Total Body HIIT Program
- Registration Number
- NCT05542758
- Lead Sponsor
- Creighton University
- Brief Summary
This study will examine differences in a 12 week high-intensity interval training regimen. The Total Body HIIT program incorporates a resistance (circuit) and an anaerobic (bike) component in older adults. The specific objectives focus on examining cardiovascular endurance, neuromuscular function, and muscle architecture.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 60
- 65-95 years of age or older
- Physical independent (Barthel Index)
- Physician clearance to participate
- No medication changes in previous 30 days
- No structured resistance training program in previous 6 months
- Contraindications to high-intensity exercise39 (PAR-Q Questionnaire)
- Severe mental impairment (<18 on Montreal Cognitive Assessment)
- Neurodegenerative or acute neurological diagnoses (e.g., Parkinson's disease, stroke, traumatic brain injury)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Total Body HIIT Program Total Body HIIT Program This Total Body HIIT program (circuit and bike training) will involve 3 sessions per week (35-40 min on nonconsecutive days) progressed across the 12 weeks. All session will be lead by undergraduate exercise science students or doctor of physical therapy students and supervised by a physical therapist.
- Primary Outcome Measures
Name Time Method Change in Evoked Muscle Function Assessments: Evoked Peak Force from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Evoked muscle function will be assessed using electrical stimulation delivered to the superficial quadriceps femoris via a cathode-anode arrangement, with the cathode probe pressed into the femoral triangle over the femoral nerve and the anode fixed over the greater trochanter. Manual stepwise increases in stimulation will be completed until max contraction is achieved. Once max contraction is achieved, a maximal, single and doublet stimulus will be administered. The single stimulation will be used to elicit a max M-wave amplitude (defined as the max M-wave peak-to-peak amplitude). A doublet stimulus will be used to drive the muscle to maximal contraction capability to investigate the muscle contractile capability. To examine maximal contractile capacity, torque produced from the quadriceps femoris from the dynamometer during the first 50 ms, evoked peak force.
Change in Voluntary Electromechanical Delay from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention To examine muscle activation, surface electromyographic (sEMG) signals collected during the voluntary and evoked muscle contractions will be collected from the quadriceps femoris (vastus lateralis, rectus femoris, and vastus medialis muscles), hamstrings (biceps femoris muscle), biceps brachii, and triceps brachii muscles. Peak muscle activation will be assessed as the peak sEMG amplitude. Voluntary electromechanical delay will be calculated from the time difference from the onset of sEMG to the onset of force.
Change in Rate of Muscle Activation from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention To examine muscle activation, surface electromyographic (sEMG) signals collected during the voluntary and evoked muscle contractions will be collected from the quadriceps femoris (vastus lateralis, rectus femoris, and vastus medialis muscles), hamstrings (biceps femoris muscle), biceps brachii, and triceps brachii muscles. Peak muscle activation will be assessed as the peak sEMG amplitude. Rate of muscle activation will be assessed in the first 50 ms following muscle activation onset.
Change in Voluntary Muscle Strength Tests (Isokinetics) from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Isokinetic strength testing on the hamstrings, quadriceps femoris, biceps brachii, and triceps brachii muscles at slow (60° per second), medium (180° per second), fast (300° per second) and fast unweighted (500° per second) speeds with three maximal repetitions performed for each speed to determine voluntary peak torque production capabilities at each speed using a dynamometer. During the strength testing assessments, each subject will be asked to push or pull "as hard as possible" against a lever arm on the dynamometer until the limb reaches the end of the range of motion.
Change in Evoked Muscle Function Assessments: Evoked Peak Rate of Force Development from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Evoked muscle function will be assessed using electrical stimulation delivered to the superficial quadriceps femoris via a cathode-anode arrangement, with the cathode probe pressed into the femoral triangle over the femoral nerve and the anode fixed over the greater trochanter. Manual stepwise increases in stimulation will be completed until max contraction is achieved. Once max contraction is achieved, a maximal, single and doublet stimulus will be administered. The single stimulation will be used to elicit a max M-wave amplitude (defined as the max M-wave peak-to-peak amplitude). A doublet stimulus will be used to drive the muscle to maximal contraction capability to investigate the muscle contractile capability. To examine maximal contractile capacity, evoked peak rate of force development 0-50ms will be recorded resulting from a maximal doublet stimulus from the quadriceps femoris.
Change in Muscle Biopsy-based Muscle Architecture from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Muscle biopsies will be collected to determine myofiber size from the quadriceps femoris (i.e., vastus lateralis). After necessary biopsy preparations, the distribution of myofiber type and size will be determined within each sample.
Change in 6-Min Walk Test performance from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention The 6MWT will be assessed by tallying the number of laps a participant is able walk on a 100 ft straight path. Partially completed laps will be measured and added to the total distance. Participants will be allowed to take standing rest breaks, if necessary, but the time will continue during all rest breaks. Participants will be instructed to "cover as much ground as you can in 6 minutes".
Change in Voluntary Muscle Strength Tests (Isometrics) from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Isometric strength of the hamstrings, quadriceps femoris, biceps brachii, and triceps brachii muscles will be assessed using a dynamometer. For maximal voluntary isometric contraction assessments, participants will complete two, 3- to 4-second MVICs of the hamstrings, quadriceps femoris, biceps brachii, and triceps brachii. Participants will be instructed to "push or pull as hard and fast as possible" and hold against the dynamometer to achieve max voluntary torque and rate of torque development.
Change in Ultrasound-based Muscle Architecture: Cross-sectional Area from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Ultrasound images of the vastus lateralis, rectus femoris, biceps femoris, vastus medialis, biceps brachii, and triceps brachii will be obtained. Muscle cross-sectional area for each muscle will be assessed.
Change in Ultrasound-based Muscle Architecture: Echo Intensity from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Ultrasound images of the vastus lateralis, rectus femoris, biceps femoris, vastus medialis, biceps brachii, and triceps brachii will be obtained. Echo intensity for each muscle will be assessed.
- Secondary Outcome Measures
Name Time Method Change in Functional Lower Body Strength from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Functional lower body strength will be assessed with the 5 times sit to stand test. This test requires participants to stand up and sit down 5 times without the use of upper extremities as fast as possible.
Change in Functional Upper Body Strength from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Functional upper body strength will be assessed with hand grip strength. Three repetitions of 30 second maximum hold on each hand will be completed.
Change in V02 peak from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Participants will complete a graded exercise test (2-min stages) on the cycle ergometer to evaluate VO2 peak. VO2 peak for each subject will be taken as the highest single VO2 value when at least two of the three following test criteria are satisfied: 1) A leveling off in VO2 despite an increase in power output, 2) maximal heart rate within 15 beats of age-predicted maximal heart rate (220-age), and 3) respiratory exchange ratio (RER) ≥1.1.
Change in Gait Speed from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Gait speed will be assessed with the 10-meter walk test (maximum comfortable walking speed).
Change in Balance: Center of Pressure Excursion from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Participants will statically stand on a force plate in three different scenarios (feet together eyes open, feet together eyes shut, and single-leg stance). Center of pressure excursion will be calculated to determine static balance.
Change in Balance: Functional Gait Assessment from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Participants will complete the functional gait assessment, a clinical assessment of walking ability under various conditions (e.g., stepping over an obstacle, walking backwards, etc.). Scores range from 0-30 with higher scores indicating better balance performance.
Change in Balance: Berg Balance Scale from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Participants will complete the Berg Balance Scale, a clinical assessment of static and dynamic balance abilities. The Berg Balance Scale Score ranges from 0-56 with higher scores indicating better balance performance.
Change in Health-Related Quality of Life from baseline to following HIIT intervention change from baseline to immediately after the HIIT intervention Participants will complete the Short-Form Health Survey (SF-36) to assess health-related quality of life.
Trial Locations
- Locations (1)
Creighton University
🇺🇸Omaha, Nebraska, United States