Arkansas Colleges of Health Education
Fort Smith, Arkansas, 72916, United States
NCT Number: NCT05951985
Individuals with and without neurologic diagnoses greatly benefit from participation in regular exercise but the majority are physically inactive. This is an issue for both them and their care partners as their health is often linked. This study aims to examine the long-term physical and psychosocial effects of structured, group-based, high intensity functional training (HIFT) exercise for people with neurologic diagnoses and their care partners.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Fort Smith, Arkansas, 72916, United States
Over the course of two years, this study will provide no-cost, twice weekly, group-based, HIFT exercise for people with neurologic diagnoses and their care partners. All participants will be required to have physician or advanced practice provider clearance to exercise. All participants will be evaluated by a physical therapist at no-cost prior to beginning the intervention to assess eligibility for the study. All eligible participants will complete a demographics questionnaire, questionnaires regarding physical and psychosocial health, and a battery of physical tests assessing mobility, strength, endurance, and balance. Participants' physical activity levels will also be monitored throughout the study through accelerometers.
Participants will participate in a maximum of twice weekly HIFT exercise for up to 2 years. All exercise programming will be led by licensed physical therapists with assistance from Doctor of Physical Therapy students. All exercise staff will be Cardiopulmonary resuscitation/basic life support certified and an automated external defibrillator will be available onsite. Exercise classes will utilize HIFT, which includes various exercises that are functional and to be performed at a high intensity. Exercises will include aerobic, resistance, and/or balance training and align with the 2018 Physical Activity Guidelines for Americans.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Exercise sessions will be 60 to 75 minutes in duration and be a combination of resistance, aerobic, and balance exercise, with emphasis on functional movements performed at a high intensity. Exercises will be tailored/modified to meet the needs of each participant.
Time frame: After 24 months of intervention
The percentage of intervention sessions attended by participants.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Lower extremity strength will be measured via functional test (Five Times Sit to Stand). This test records the amount of time taken to rise and sit to and from a chair five consecutive times. Faster times indicate greater lower extremity strength.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
The PDQ-39 is a 39-item participant-reported questionnaire which assesses health-related quality of life across 8 domains (mobility, activities of daily living, emotional well-being, stigma, social support, cognition, communication, bodily discomfort). Participants respond to each item using a 5-point Likert scale from 0 (never) to 4 (always). Items in each domain are scored by expressing summed item scores as a percentage (ranging from 0 to 100%). Lower scores indicate better quality of life.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Fast-paced walking speed will be measured via 10 meter walk test, which has individuals walk 10 meters with the middle 6 meters timed; two trials are performed and the average time is taken. Faster walking speeds indicate greater mobility with walking.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Fast-paced propulsion speed will be measured via wheelchair propulsion test, which has individuals propel 10 meters and are timed; two trials are performed and the average time is taken. Faster propulsion speeds indicate greater mobility with wheelchair propulsion.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
The 6 Minute Walk Test measures a participants ability to cover as much distance (measured in meters) as possible while walking for 6 minutes. Participants will walk along a pre-defined pathway for 6 minutes, resting as needed. The test is a measure of walking endurance with further distances indicating greater endurance.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
The 6 Minute Propulsion Test measures a participants ability to cover as much distance (measured in meters) as possible while propelling a wheelchair for 6 minutes. The test is a measure of aerobic endurance with further distances indicating greater endurance.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
The MDS-UPDRS measures disability as a result of Parkinson's and allows tracking for progression of the disease. The scale has four parts (1, mentation, behavior and mood, 2, activities of daily living, 3, motor examination, and 4, complications of therapy. Each parkinsonian sign or symptom is ranked on a 5-point Likert scale (ranging from 0 to 4) with higher scores indicating greater impairments. The minimum score on the entire scale is 0 and the maximum is 199.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Physical activity levels will be measured via thigh or wrist-worn accelerometer (activPAL or ActiGraph). These small devices will be worn on the less affected thigh or wrist (or non-dominant thigh or wrist for care partners). Through collecting acceleration data, different intensities of physical activity will be inferred (i.e light, moderate and vigorous intensity physical activity), with moderate-to-vigorous intensity physical activity being used as the primary outcome measure. At all time points, participants will wear the accelerometer for 7 consecutive days.
Time frame: After 24 months of intervention
The number and percentage of participants who remain in the study through the final measurement point at 24 months.
Time frame: Throughout the 24 months study period
The number of participants recruited will be reported as a percentage of total participants contacted for study participation.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
The four square step test measures stepping balance as the time taken to step clockwise and counterclockwise in a square pattern. Faster times indicate greater balance.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
The YMCA Bench Press Test measures muscular endurance of the upper body. The test requires participants to complete as many repetitions of barbell bench press as they can with good form. Greater number of repetitions indicates greater muscular endurance.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
The 30 second peak power test measures anaerobic power produced (in watts) over 30 seconds on a ski ergometer. Greater wattage indicates greater anaerobic power.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Change will be reported using a visual analogue scale where participants rate their confidence from not confident at all to completely confident.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Change will be reported using a visual analogue scale where participants rate their pain from no pain to worst possible pain.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Change will be reported using a visual analogue scale where participants rate their sleep quality from poor to exceptional.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Change will be reported using a visual analogue scale where participants rate their level of social support from people in the intervention and those outside the intervention. The scale goes from poor to exceptional social support.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Change will be reported using a visual analogue scale where participants rate their level of ability from poor to exceptional on attributes of mobility, power, endurance/stamina, strength and balance.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Using a visual analogue scale, participants rate their feelings of safety with the intervention at 24 months. Scores range from not safe at all to exceptionally safe.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Using a visual analogue scale, participants rate their feelings of satisfaction with coach supervision during the intervention at 24 months. Scores range from not satisfied at all to extremely satisfied.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Using a visual analogue scale, participants rate their feelings of inclusion during the intervention at 24 months. Scores range from minimally included to maximally included.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Using a visual analogue scale, participants rate their feelings of exercise intensity during the intervention at 24 months. Scores range from low intensity to high intensity exercise.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Using a visual analogue scale, participants rate their feelings on exercise variety during the intervention at 24 months. Scores range from low exercise variety to high exercise variety.
Time frame: After, 3, 6, 9, 12, 15, 18, 21 and 24 months of intervention
Using a visual analogue scale, participants rate their feelings on applicability of exercises to real life during the intervention at 24 months. Scores range from not applicable at all to extremely applicable.
Arkansas Colleges of Health Education
Other
High Intensity Functional Training for Individuals With Neurologic Diagnoses and Their Care Partners: A 2-Year Longitudinal Study
Acronym: SHIFT-AR
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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