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The purpose of this research study is to better understand how exercise training in older adults (≥65 years) with heart failure (HF) affects skeletal muscle both intrinsically and in respect to its impact on functional capacity. While many conceptualize HF as a pathophysiology that exclusively affects the heart, skeletal muscle atrophy and weakening are also elemental to the disease. While reduced exercise capacity is typically associated with HF, this may be related more to disease effects in skeletal muscle than the heart. This is a clinical study that focuses on exercise training which compares functional endpoints before and after training. Patients are randomized to one of three exercise training interventions (aerobic vs. aerobic and strength vs. inspiratory muscle training) for 12 weeks and are assessed pre- and post-training to determine if any differences occur in their skeletal muscle and functional capacity. Skeletal muscle biopsies before and after the exercise training intervention in order to study changes in skeletal muscle histology and biology.
Functional endpoints in this study include ventilatory gas indices from cardiopulmonary exercise testing, lower body strength testing, grip strength, sit-to-stand, six-minute-walk distance, gait speed, inspiratory muscle strength, and quality of life and physical activity-oriented questionnaires, including the Kansas City Cardiomyopathy Questionnaire, Duke Activity Status Index, and CHAMPS Physical Activity Questionnaire for Older Adults. Body composition is measured with Dual Energy X-ray (DXA) scanning. Skeletal muscle biopsies are completed in the vastus lateralis of the non-dominant leg to assess histology and biologic endpoints.
Despite decades of research, HF remains a common disease that continues to rise in prevalence, particularly among the expanding population of older adults. By virtue of age, older adults are prone to higher incidence of HF and worse clinical consequences. Exercise intolerance and dyspnea are common symptoms that portend poor prognosis, and which erode functional independence and quality of life. Mortality and morbidity also increase significantly as functional capacity declines.
Growing evidence suggests that pathophysiology of central cardiac dysfunction is linked to skeletal muscle pathophysiology. While HF therapeutic guidelines primarily emphasize steps that improve cardiac parameters, and/or volume status, goals to modify HF skeletal muscle myopathy may constitute a vital complementary treatment target.
Ongoing analyses from our pilot VA Merit investigation provide pertinent insights and substantiation. The investigators demonstrated reduced functional capacity (both aerobic and strength) in 31 HF patients (mean age 66 years) compared to 39 age-matched healthy controls (mean age 67). The investigators also showed increased expression of genes signaling ubiquitin-mediated proteolysis in skeletal muscle in relation to decreasing aerobic and strength performance. Consistently, reduced lean muscle mass, as measured by DXA, correlated to the reduced strength indices.
This proposal constitutes a logical progression of this pilot analysis and follows the analytic path the investigators anticipated. Whereas the initial work characterized key skeletal muscle gene expression patterns in association to disease, exercise capacity, and body composition, this study compares the effects of three exercise training regimens (i.e., aerobic vs. combined aerobic and strength vs. inspiratory muscle training [IMT]) each with a unique physiological rationale. The investigators will explore differences in how each training regimen modifies clinical attributes (function/symptoms) as well as skeletal muscle biology that likely underlie these differences. These insights will help identify therapeutic strategies that better suppress injurious disease mechanisms and thereby facilitate improved clinical outcomes and quality of life.
Specific Aims:
a. To assess differences in functional outcomes (peak oxygen utilization [VO2]) and one-repetition max [1RM]) relative to different training regimens: a. Aerobic vs. Aerobic-Strength vs. inspiratory Muscle Training (IMT).
i. Analyses will include assessments of training differences in respect to broader functional parameters (aerobic, strength, inspiration), symptoms, and quality of life.
b. To assess gene expression in relation to the different training regimens.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Aerobic Exercise Intervention | Other | 12 weeks of a minimum of 3 days a week for 60 minutes of aerobic exercise |
|
| Combined Aerobic and Strength Exercise Intervention | Other | 12 weeks of a minimum of 3 days a week for 60 minutes of Combined Aerobic and Strength Exercise |
|
| Inspiratory Muscle Training Exercise Intervention | Other | 12 weeks of a minimum of 3 days a week for 60 minutes of Inspiratory Muscle Training Exercise |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Aerobic Exercise Intervention | Behavioral | Aerobic Exercise Intervention - 12 weeks of a minimum of 3 days a week for 60 minutes of aerobic exercise |
|
| Measure | Description | Time Frame |
|---|---|---|
| Oxygen Uptake (VO2) Peak | a cardiopulmonary exercise test will be performed to determined peak VO2 in ML/KG/Min | baseline and through study completion an average of 14 weeks |
| One Repetition Maximum- Leg Press | Leg press will be performed on the Keiser Leg press and measured in kilograms (kg) | baseline and through study completion an average of 14 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Metabolomics | Nitric Oxide Bioavailability (uM) Metabolomics The scientific direction of our analyses for this measure has shifted over time. The investigators will pursue RNA seq and metabolomics to provide an unbiased path forward on viable targets in the muscle. | baseline and through study completion an average of 14 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Inflammation - C-reactive Protein | Inflammation - C-reactive protein (CRP) will be measured through blood | baseline and through study completion an average of 14 weeks |
| Dual-energy X-ray Absorptiometry |
Inclusion Criteria:
Exclusion Criteria:
Major cardiovascular event or procedure within the prior 6 weeks.
Dementia
Severe COPD (FEV1<50%),
End-stage malignancy
Severe valvular heart disease that would make exercise un safe
Orthopedic limitation preventing exercise
Any bleeding disorder that would contraindicate safe exercise
Women who are pregnant, breastfeeding, or likely to become pregnant within the next 6 months
Psychiatric hospitalization within the last 3 months
ICD device with heart rate limits that prohibit exercise assessments or exercise training.
Chronic use of oral corticosteroids or medications that affect muscle function.
Chronic ETOH or drug dependency shown within the last year
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| Name | Affiliation | Role |
|---|---|---|
| Daniel E. Forman, MD | VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA | Boston | Massachusetts | 02130 | United States | ||
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65 participants consented to enroll in the study. 45 participants completed a baseline assessment and were randomized to one of the three intervention arms.
The remaining 20 participants withdrew prior to completing baseline and before being randomized to one of the three intervention arms, so they are not included in this table. Serious adverse events reported after consent but prior to withdrawal for the non-randomized participants are included in a separate group in the adverse events table.
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| ID | Title | Description |
|---|---|---|
| FG000 | Aerobic Exercise Intervention | Participants completed a 12-week exercise training regimen consisting of aerobic exercise for a minimum of 60 minutes in length three times a week. |
| FG001 | Combined Aerobic and Strength Exercise Intervention |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Mar 30, 2020 |
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Participants with heart failure will complete 1 of 3 exercise training interventions (aerobic vs. aerobic and strength vs. inspiratory) for 12 weeks and will be assessed pre and post to determine if any differences occur in their skeletal muscle and functional capacity as part of the exercise intervention.
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| Combined Aerobic and Strength Exercise Intervention | Behavioral | Combined Aerobic and Strength Exercise Intervention- 12 weeks of a minimum of 3 days a week for 60 minutes of Combined Aerobic and Strength Exercise |
|
| Inspiratory Muscle Training Exercise Intervention | Behavioral | Inspiratory Muscle Training Exercise Intervention- 12 weeks of a minimum of 3 days a week for 60 minutes of Inspiratory Muscle Training Exercise |
|
| Skeletal Muscle Gene Expression |
Skeletal muscle gene expression will be measured in RNA isolated from skeletal muscle biopsy samples via Illumina platform. The measure "Number" indicates the number of differentially expressed genes, and units are fold change over baseline. To investigate how the lifestyle interventions impacted gene expression at the mRNA level in skeletal muscles of our research participants we performed high-throughput RNA-Sequencing (Illumina HiSeq paired-end 150 base pairs). Differential gene expression analysis was performed on the RNA-seq. data using DeSEQ2 to determine differentially expressed genes (DEGs) between groups. All DEG analyses were performed using the Wald test (p < 0.05) corrected for multiple comparisons using the Benjamini and Hochberg method. |
| baseline and through study completion an average of 14 weeks |
| Quality of Life and Daily Function Questionnaires | Participants completed the Kansas City Cardiomyopathy questionnaire (KCCQ) and Duke Activity Status (DASI) Index standardized questionnaires. The KCCQ is scored on a scale of 0 to 100 with a higher score representing better health status. DASI is a 12-item questionnaire that is scored on a scale of 0 to 58.2, with a higher score representing a higher functional status. | baseline and through study completion an average of 12 weeks |
| Community Healthy Activities Model Program for Seniors (CHAMPS) Physical Activity Questionnaire for Older Adults - Frequency Component | Participants completed the Community Healthy Activities Model Program for Seniors (CHAMPS) Physical Activity Questionnaire for Older Adults as part of the Quality of Life and Daily Function study outcome. The CHAMPS questionnaire assesses duration and frequency of self-reported weekly physical activities of varying intensities in older adults. One component of the CHAMPS score is the frequency per week (i.e. number or count of events per week) that the participant reported that they engaged in all exercise related activities, and the frequency per week that the participant engaged in moderate-vigorous activities. The mean frequency of activities per week at baseline and follow-up for each study arm are reported here for the participants who completed both a baseline and follow-up assessment. A higher mean indicates a higher number of exercise-related activities were reported per week. | baseline and through study completion an average of 12 weeks |
| Community Healthy Activities Model Program for Seniors (CHAMPS) Physical Activity Questionnaire for Older Adults - Duration Component | Participants completed the Community Healthy Activities Model Program for Seniors (CHAMPS) Physical Activity Questionnaire for Older Adults as part of the Quality of Life and Daily Function study outcome. The CHAMPS questionnaire assesses duration and frequency of self-reported weekly physical activities of varying intensities in older adults. One component of the CHAMPS score is the self-reported duration in hours per week of all exercise-related activities, and duration in hours per week of moderate-vigorous exercise-related activities. The mean duration of all exercise-related activities and moderate-vigorous activities in hours per week are reported here for participants in each study arm who completed both the baseline and 12 week follow-up assessments. A higher mean indicates that a longer duration of exercise-related activities in hours per week were reported. | baseline and through study completion an average of 12 weeks |
dual-energy x-ray absorptiometry will look at muscle mass change in kg
| Baseline and through study completion an average of 14 weeks |
| VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA |
| Pittsburgh |
| Pennsylvania |
| 15240 |
| United States |
Participants completed a 12-week exercise training regimen consisting of combined aerobic and strength exercise for a minimum of 60 minutes in length three times a week. |
| FG002 | Inspiratory Muscle Training Exercise Intervention | Participants completed a 12-week exercise training regimen consisting of inspiratory muscle training exercise for a minimum of 60 minutes in length three times a week. |
| COMPLETED |
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| NOT COMPLETED |
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65 participants consented to enroll in the study. Baseline demographics were captured for 48 of the participants who consented.
20 participants who consented to participate withdrew consent prior to completing baseline and prior to randomization. Baseline data were captured for 7 of these 20 participants prior to withdrawal.
45 participants completed baseline and were randomized to one of the three study arms. Baseline demographics were missing for 4 of these 45 randomized participants.
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| ID | Title | Description |
|---|---|---|
| BG000 | Aerobic Exercise Intervention | Participants completed a 12-week exercise training regimen consisting of aerobic exercise for a minimum of 60 minutes in length three times a week. |
| BG001 | Combined Aerobic and Strength Exercise Intervention | Participants completed a 12-week exercise training regimen consisting of combined aerobic and strength exercise for a minimum of 60 minutes in length three times a week. |
| BG002 | Inspiratory Muscle Training Exercise Intervention | Participants completed a 12-week exercise training regimen consisting of inspiratory muscle training exercise for a minimum of 60 minutes in length three times a week. |
| BG003 | Consented But Withdrew Pre-randomization | This group includes participants who consented to enroll in the study, but only completed partial or no baseline functional or questionnaire assessments, and then withdrew from the study prior to being randomized. Therefore these participants were not randomly assigned to one of the three study arms, but baseline demographic data were collected after consent and prior to randomization. The baseline demographic data are included here for completion. |
| BG004 | Total | Total of all reporting groups |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean | Standard Deviation | years |
| |||||||||||||||
| Sex: Female, Male | Count of Participants | Participants |
| ||||||||||||||||
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Oxygen Uptake (VO2) Peak | a cardiopulmonary exercise test will be performed to determined peak VO2 in ML/KG/Min | Pre and post peak VO2 data available for 33 of 45 randomized participants. Remaining randomized participants did not complete a post assessment so are excluded from the table. | Posted | Mean | Standard Deviation | ML/KG/Min | baseline and through study completion an average of 14 weeks |
|
|
| ||||||||||||||||||||||||||||||||
| Primary | One Repetition Maximum- Leg Press | Leg press will be performed on the Keiser Leg press and measured in kilograms (kg) | Data available for 30 of 45 randomized participants who completed both a pre and post assessment. | Posted | Mean | Standard Deviation | kg | baseline and through study completion an average of 14 weeks |
| ||||||||||||||||||||||||||||||||||
| Secondary | Metabolomics | Nitric Oxide Bioavailability (uM) Metabolomics The scientific direction of our analyses for this measure has shifted over time. The investigators will pursue RNA seq and metabolomics to provide an unbiased path forward on viable targets in the muscle. | Nitric oxide bioavailability metabolomics data were collected for 23 of the participants at both the baseline and follow-up assessments. | Posted | Mean | Standard Deviation | micrometer (uM) | baseline and through study completion an average of 14 weeks |
| ||||||||||||||||||||||||||||||||||
| Secondary | Skeletal Muscle Gene Expression | Skeletal muscle gene expression will be measured in RNA isolated from skeletal muscle biopsy samples via Illumina platform. The measure "Number" indicates the number of differentially expressed genes, and units are fold change over baseline. To investigate how the lifestyle interventions impacted gene expression at the mRNA level in skeletal muscles of our research participants we performed high-throughput RNA-Sequencing (Illumina HiSeq paired-end 150 base pairs). Differential gene expression analysis was performed on the RNA-seq. data using DeSEQ2 to determine differentially expressed genes (DEGs) between groups. All DEG analyses were performed using the Wald test (p < 0.05) corrected for multiple comparisons using the Benjamini and Hochberg method. | Skeletal muscle samples were collected for 19 participants who completed both a baseline and follow-up assessment. | Posted | Number | Fold change over baseline | baseline and through study completion an average of 14 weeks |
| |||||||||||||||||||||||||||||||||||
| Secondary | Quality of Life and Daily Function Questionnaires | Participants completed the Kansas City Cardiomyopathy questionnaire (KCCQ) and Duke Activity Status (DASI) Index standardized questionnaires. The KCCQ is scored on a scale of 0 to 100 with a higher score representing better health status. DASI is a 12-item questionnaire that is scored on a scale of 0 to 58.2, with a higher score representing a higher functional status. | Questionnaire data available for 32 participants who completed both the baseline and 12-week follow-up assessments. | Posted | Mean | Standard Deviation | scores on a scale | baseline and through study completion an average of 12 weeks |
| ||||||||||||||||||||||||||||||||||
| Secondary | Community Healthy Activities Model Program for Seniors (CHAMPS) Physical Activity Questionnaire for Older Adults - Frequency Component | Participants completed the Community Healthy Activities Model Program for Seniors (CHAMPS) Physical Activity Questionnaire for Older Adults as part of the Quality of Life and Daily Function study outcome. The CHAMPS questionnaire assesses duration and frequency of self-reported weekly physical activities of varying intensities in older adults. One component of the CHAMPS score is the frequency per week (i.e. number or count of events per week) that the participant reported that they engaged in all exercise related activities, and the frequency per week that the participant engaged in moderate-vigorous activities. The mean frequency of activities per week at baseline and follow-up for each study arm are reported here for the participants who completed both a baseline and follow-up assessment. A higher mean indicates a higher number of exercise-related activities were reported per week. | Questionnaire data available for 32 participants who completed both the baseline and 12-week follow-up assessments. The mean at baseline and 12-week follow-up are reported. | Posted | Mean | Standard Deviation | events per week | baseline and through study completion an average of 12 weeks |
| ||||||||||||||||||||||||||||||||||
| Secondary | Community Healthy Activities Model Program for Seniors (CHAMPS) Physical Activity Questionnaire for Older Adults - Duration Component | Participants completed the Community Healthy Activities Model Program for Seniors (CHAMPS) Physical Activity Questionnaire for Older Adults as part of the Quality of Life and Daily Function study outcome. The CHAMPS questionnaire assesses duration and frequency of self-reported weekly physical activities of varying intensities in older adults. One component of the CHAMPS score is the self-reported duration in hours per week of all exercise-related activities, and duration in hours per week of moderate-vigorous exercise-related activities. The mean duration of all exercise-related activities and moderate-vigorous activities in hours per week are reported here for participants in each study arm who completed both the baseline and 12 week follow-up assessments. A higher mean indicates that a longer duration of exercise-related activities in hours per week were reported. | Questionnaire data available for 32 participants who completed both the baseline and 12-week follow-up assessments. The mean at baseline and 12-week follow-up are reported. | Posted | Mean | Standard Deviation | hours per week | baseline and through study completion an average of 12 weeks |
| ||||||||||||||||||||||||||||||||||
| Other Pre-specified | Inflammation - C-reactive Protein | Inflammation - C-reactive protein (CRP) will be measured through blood | Data for the C-reactive protein outcome was collected for 28 participants. | Posted | Mean | Standard Deviation | mg/L | baseline and through study completion an average of 14 weeks |
| ||||||||||||||||||||||||||||||||||
| Other Pre-specified | Dual-energy X-ray Absorptiometry | dual-energy x-ray absorptiometry will look at muscle mass change in kg | 23 randomized participants completed baseline dual-energy x-ray absorptiometry, and 15 of those completed the follow-up scan. | Posted | Mean | Standard Deviation | kg | Baseline and through study completion an average of 14 weeks |
|
After consent through study completion, up to 12 weeks
Serious Adverse Events (SAEs) were reported for participants who consented to the study and were therefore considered enrolled. Some participants experienced an adverse event after consent but prior to completing the full baseline assessments, and withdrew from the study before they were randomized to one of the three intervention arms. For completion, the SAEs reported for these participants are listed in a separate "consented but withdrew pre-randomization" column.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Aerobic Exercise Intervention | Participants completed a 12-week exercise training regimen consisting of aerobic exercise for a minimum of 60 minutes in length three times a week. | 0 | 16 | 10 | 16 | 0 | 16 |
| EG001 | Combined Aerobic and Strength Exercise Intervention | Participants completed a 12-week exercise training regimen consisting of combined aerobic and strength exercise for a minimum of 60 minutes in length three times a week. | 0 | 17 | 3 | 17 | 0 | 17 |
| EG002 | Inspiratory Muscle Training Exercise Intervention | Participants completed a 12-week exercise training regimen consisting of inspiratory muscle training exercise for a minimum of 60 minutes in length three times a week. | 0 | 12 | 5 | 12 | 1 | 12 |
| EG003 | Consented But Withdrew Pre-randomization | Participants who consented to enroll in the study, but only completed partial or no baseline assessments and then withdrew from the study prior to being randomized. These participants were not assigned to one of the three study arms, but had adverse event data that was reported after their consent and prior to withdrawal. | 0 | 5 | 5 | 5 | 0 | 5 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Influenza | Infections and infestations | Non-systematic Assessment | Hospitalization, unrelated to study |
| |
| Gout | Musculoskeletal and connective tissue disorders | Non-systematic Assessment | ED, unrelated to study |
| |
| Chest wall pain | Musculoskeletal and connective tissue disorders | Non-systematic Assessment | ED, unrelated to study |
| |
| Eye Surgery | Surgical and medical procedures | Non-systematic Assessment | Pre-planned, unrelated to study |
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| Shoulder fracture | Musculoskeletal and connective tissue disorders | Non-systematic Assessment | ED, unrelated to study |
| |
| Hyponatremia | Metabolism and nutrition disorders | Non-systematic Assessment | Hospitalization, unrelated to study |
| |
| Mechanical Fall with Fractures | Musculoskeletal and connective tissue disorders | Non-systematic Assessment | Hospitalization, unrelated to study |
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| Acute Heart Failure | Cardiac disorders | Non-systematic Assessment | Hospitalization, unrelated to study |
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| Feeling faint | General disorders | Non-systematic Assessment | Hospitalization, unrelated to study |
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| Acute Heart Failure | Cardiac disorders | Non-systematic Assessment | Hospitalization, unrelated to study |
| |
| Hypertension | Cardiac disorders | Non-systematic Assessment | Referral, unrelated to study |
| |
| LV thrombus | Cardiac disorders | Non-systematic Assessment | Follow-up, unrelated to study |
| |
| Stomach, Chest pain | General disorders | Non-systematic Assessment | ED, unrelated to study |
| |
| Shoulder pain after fall on ice | Musculoskeletal and connective tissue disorders | Non-systematic Assessment | ED, unrelated to study |
| |
| Chest Pain | Cardiac disorders | Non-systematic Assessment | Hospitalization, unrelated to study |
| |
| dizziness, SOB, fogginess after medication change | General disorders | Non-systematic Assessment | ED, unrelated to study |
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| Unknown Respiratory Disorder | Respiratory, thoracic and mediastinal disorders | Non-systematic Assessment | Hospitalization, unrelated to study |
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| Hypotension | Cardiac disorders | Non-systematic Assessment | Hospitalization, unrelated to study |
| |
| Mechanical fall on head | Musculoskeletal and connective tissue disorders | Non-systematic Assessment | Hospitalization, unrelated to study |
| |
| Hypoglycemia | Endocrine disorders | Non-systematic Assessment | ED, unrelated to study |
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| Constipation | Gastrointestinal disorders | Non-systematic Assessment | ED, unrelated to study |
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| Thigh skin flap removal | Skin and subcutaneous tissue disorders | Non-systematic Assessment | Pre-planned, unrelated to study |
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| Lightheadedness after starting new medication | General disorders | Non-systematic Assessment | ED, unrelated to study |
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| Atrial fibrillation | Cardiac disorders | Non-systematic Assessment | Hospitalization, unrelated to study |
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| Edema | General disorders | Non-systematic Assessment | ED, unrelated to study |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Spinal stenosis | Musculoskeletal and connective tissue disorders | Non-systematic Assessment | ED, unrelated to study |
|
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Daniel E. Forman, MD | VA Pittsburgh Healthcare System | (412) 360-2917 | Daniel.Forman@va.gov |
| Feb 3, 2023 |
| Prot_SAP_000.pdf |
| ID | Term |
|---|---|
| D006333 | Heart Failure |
| D009043 | Motor Activity |
| ID | Term |
|---|---|
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D001519 | Behavior |
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| Male |
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| Asian |
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| Native Hawaiian or Other Pacific Islander |
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| Black or African American |
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| White |
|
| More than one race |
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| Unknown or Not Reported |
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| Units |
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| Counts |
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| Participants |
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| OG002 | Inspiratory Muscle Training Exercise Intervention | Participants completed a 12-week exercise training regimen consisting of inspiratory muscle training exercise for a minimum of 60 minutes in length three times a week. |
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Participants completed a 12-week exercise training regimen consisting of combined aerobic and strength exercise for a minimum of 60 minutes in length three times a week. |
| OG002 | Inspiratory Muscle Training Exercise Intervention | Participants completed a 12-week exercise training regimen consisting of inspiratory muscle training exercise for a minimum of 60 minutes in length three times a week. |
|
|
Participants completed a 12-week exercise training regimen consisting of combined aerobic and strength exercise for a minimum of 60 minutes in length three times a week. |
| OG002 | Inspiratory Muscle Training Exercise Intervention | Participants completed a 12-week exercise training regimen consisting of inspiratory muscle training exercise for a minimum of 60 minutes in length three times a week. |
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| Participants |
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