Parkinson's DiseasePhase 2NCT02230267
High-intensity Exercise and Fall Prevention Boot Camp for Parkinson's Disease
A Phase 2 study testing High intensity exercise and balance training in people with Parkinson's Disease, run by University of Nevada, Las Vegas at 1 site in United States.
Trial summary
Several animal and human epidemiologic studies have provided evidence that exercise may be neuroprotective in Parkinson's disease (PD). Exercise may forestall diagnosis and, in the case of those who have already been diagnosed with PD, it may slow the observed neurodegeneration. Read more about this study
- Who is it for?
- Ages 45 to 85 years
- Conditions the study is for
- Parkinson's Disease
- What is being tested?
- High intensity exercise and balance training
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 27 participants
- Where
- 1 siteUnited States
- Study dates
- Aug 2014to Dec 2015
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 45 to 85 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Neurologist-diagnosed idiopathic PD based on the UK PD brain bank criteria
- Aged 45-85
- Hoehn and Yahr stages 1-3 (mild to moderate PD)
- Participants do not anticipate a change in medication or surgical procedures in the next 8 months of the trial (2 months for the trial and 6 for the follow-up)
- Clearance from primary care physician to participate in the trial
- Must be stable on PD medication and DBS for 3 months prior to trial
Who cannot join
- Poorly controlled or unstable cardiovascular disease that precludes participation in exercise
- Moderate-to-severe dementia using the Montreal Cognitive Assessment (MoCA). We will exclude participants with a MoCA cut off score of <26/30. This cut off value has excellent sensitivity (90%) and specificity (75%).
- Inability to stand or walk for more than 10 minutes
- Other significant disorders that would limit endurance exercise participation (i.e., osteoarthritis, stroke, respiratory problems, traumatic brain injury, neuromuscular disease, pain)
- Already participating in a regular, vigorous exercise program (3X/week or more of >60% estimated maximum heart rate)
- Participants will be excluded from the trial if they are taking any medications that interfere with heart rate response to exercise
Trial locations and contacts
1 site in 1 country.
United States1 site
University of Nevada, Las Vegas
Las Vegas, Nevada, 89154
About this study
Several animal and human epidemiologic studies have provided evidence that exercise may be neuroprotective in Parkinson's disease (PD). Exercise may forestall diagnosis and, in the case of those who have already been diagnosed with PD, it may slow the observed neurodegeneration. Unfortunately, because this line of research is in early stages, there is little evidence to indicate what biological mechanisms underlie the neuroprotection that is conferred with exercise. Toward this end, it is possible that an interaction between endogenous antioxidant enzymes, inflammatory processes, and reactive oxygen species may be associated with exercise improvements in PD.
One of the most common reasons for premature death in PD is falls. Several meta-analyses have concluded that exercise training programs focused on balance and/or strength training are effective at improving aspects of balance. Taken together, the current body of evidence suggests that exercise may be neuroprotective and balance/strength training may decrease the likelihood of a fall. The combination of these efficacious treatment modalities (exercise and balance/strength training) in a comprehensive treatment approach to improve PD symptoms and balance has been previously reported at relatively mild or moderate exercise intensities. Because recent research has suggested that patients with PD may benefit more from more physically intense programs, we are proposing a more aggressive approach with regard to exercise intensity and frequency in the present trial. The primary purpose of this study is to determine the feasibility and safety of a high intensity exercise approach to PD. A secondary purpose is to determine the trajectory of change in outcomes over the duration of the trial from a high intensity fall prevention program. It is hoped that a signal of efficacy will allow this trial to progress to a comparative effectiveness trial. An important innovative design element is collecting biological assays to better understand the mechanism underlying the anticipated clinical improvements.
Read more
Aim 1 is to test the feasibility of a high-intensity exercise and fall prevention boot camp (HIBC) in patients with PD by analyzing adherence and whether they achieve minimum Centers for Disease Control exercise standards (150 min/wk moderate level aerobic exercise; strengthening at least two times per week) for the duration of the trial. Aim 2 is to determine if participation in an 8-week HIBC under the direction of a physical therapist is safe for individuals with PD. Secondary Aim 3 is to determine if participation in an 8-week HIBC will produce a signal of efficacy for several physical outcomes: falls per physical activity ratio, balance efficacy, motor activity, fatigue, muscle strength, bone health, cognition/mood, and quality of life. Secondary Aim 4 is to determine if participation in an 8-week HIBC will produce a signal of efficacy for biological outcomes, anti-inflammatory cytokines and anti-oxidant enzymes. An additional exploratory aim will be an analysis of BDNF val66val, val66met, met66met polymorphisms to determine if there is a differential response to exercise.
This trial is innovative because it utilizes a high intensity comprehensive exercise treatment approach (aerobic exercise, strengthening, and balance training). To our knowledge, there have been no trials of individuals with PD who have participated in a trial of this intensity in a group "boot camp" setting. Another innovative design element is the use of three novel assessments: biological assays of pro- and anti-inflammatory cytokines, endogenous anti-oxidant enzymes and a novel assessment of falls (falls per physical activity ratio).
Participants will be randomly assigned into either an 8-week HIBC group or an 8-week usual care control group (standard, low intensity group therapy class) under the direction of physical therapists. Each group will have 15 participants with a 1:5 patient-to-therapist ratio. The HIBC will be 1.5 hours daily, Monday through Friday. Participants will be required to attend 3 out of the 5 days. The protocol of the HIBC will include the following exercise components: A. 30 minutes of moderate-high intensity aerobic exercise; B. 15 minutes of strengthening the major muscle groups; C. 15 minutes of balance training; and, D. 15 minutes of interspersed rest and stretching. Participants will rotate through these four exercise components. Participants will have one baseline test and assessments at the 2-week, 4 week, 8-week, and 6-month points. Outcomes of the primary aims (Aim 1 and Aim 2) will be frequency counts of participation, adverse events, and compliance with exercise. The outcomes for the secondary aims will include measures of balance and falls, physical capacity, fatigue, exercise/physical activity behavior, and biological assays.
- Conditions
- Parkinson's Disease
- Being tested
- High intensity exercise and balance training, Usual care arm exercise
- Keywords
- boot camp, exercise, balance training, fall prevention, falling, strength training
- Medical subject headings
- Parkinson Disease, Motor Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
High intensity exercise and balance trainingOther
Also called A. 30 minutes of moderate-high intensity aerobic exercise at 70%+ of estimated maximum heart rate, B. 15 minutes of strengthening the major muscle groups of the trunk and upper/lower extremities, C. 15 minutes of balance training, D. 15 minutes of rest and stretching
Usual care arm exerciseOther
Also called 10 minutes of stretching, 10 minutes of aerobic exercise (60% of heart rate maximum), 10 minutes of strengthening
| Study group | Role | What they receive |
|---|---|---|
| High intensity boot camp | Experimental | Each of the two HIBCs will have 10 participants (20 total) with a 1:5 physical therapist-to-patient ratio. Each HIBC session will last 1.5 hours and will be held on 4 days of the week. Participants will be required to attend 3 of those 4 days but may attend all. Because this is a pragmatic trial, therapists will have some leeway to control the intensity and the modality of the exercise. However, the basic format of the HIBC will consist of the following exercise components: A. 30 minutes of moderate-high intensity aerobic exercise at 70%+ of estimated maximum heart rate; B. 15 minutes of strengthening the major muscle groups of the trunk and upper/lower extremities; C. 15 minutes of balance training; and, D. 15 minutes of rest and stretching. Participants will rotate through these four different exercise components in a circuit fashion. Receives: Other: High intensity exercise and balance training |
| Usual care arm | Active comparator | The low intensity exercise group will participate in the Fitness Counts Exercise Program (FCEP) which is a basic low intensity, sitting and standing exercise program (10 minutes of stretching, 10 minutes of aerobic exercise (60% of heart rate maximum), and 10 minutes of strengthening). This exercise program was developed by the National Parkinson Foundation and is commonly used in PD exercise classes. The physical therapist-to-patient ratio will be 1:5. As there are two clinical sites, there will be 10 participants in each of the two boot camps (20 total). The FCEP will be 1 hour daily on four days of the week. Participants will be required to attend 3 days per week but may attend more if they are able. Receives: Other: Usual care arm exercise |
What is being measured
The primary outcome is the main question the study is designed to answer.
Frequency feasibility
The number of participants that attend and participate in the treatment at least 3 times per week for 8 weeks.
Measured: After completion of the 8 week trial
Aerobic feasibility
The number of participants that complete at least 150 minutes per week of moderate intensity exercise (70%+ of their estimated HR maximum). This will be ascertained using heart rate monitors.
Measured: At the end of the 8 week trial
Strength feasibility
The number of participants that participate in strengthening exercises that incorporates all the major muscle groups at least two days per week.
Measured: At the end of the 8 week trial
Compliance
Drop-out rate and reason for drop-out will be tracked.
Measured: At the end of the 8 week trial
Safety
Exercise-related adverse events (e.g., strains/sprains, cardiovascular events).
Measured: Ongoing throughout the 8 week trial
Motivation
The Intrinsic Motivation Inventory (IMI) will be used to gather information about motivation.
Measured: At 8 weeks
Falls
Falls and fall injuries in and out of boot camp will be collected.
Measured: At the end of the 8 week trial
Secondary outcomes (19)
Falls
Falls will be tracked for 6 months after the boot camp using a falls diary. A member of the research team will call each month to interview participants about their falls. We will assess falls/fall injuries per physical activity ratio during the 6 month period following the trial and time to a fall/fall injury after the trial.
Measured: up to 6 months
Motor activity
Physical activity will be assessed using the Physical Activity Monitoring System (PAMsys).
Measured: up to 6 months
Fatigue
Fatigue will be assessed using the Parkinson Fatigue Scale (PFS).
Measured: up to 6 months
Strength
This will be assessed functionally using the 30 second Sit-To-Stand Test (30STS) for muscle strength.
Measured: up to 6 months
Cognition
Cognition will be assessed using the Montreal Cognitive Assessment (MoCA).
Measured: up to 6 months
Quality of life
This will be assessed by using a measure of disease-specific quality of life (Parkinson's Disease Questionnaire-39 (PDQ39)).
Measured: up to 6 months
Long term behavioral change
All participants will track their participation in exercise and physical activity using an exercise diary for 6 months following the boot camp. Participants will be called monthly to reinforce completion of the exercise diary.
Measured: up to 6 months
mini-Balance Evaluation Systems Test (mini-BESTest)
Performance-based balance tasks.
Measured: up to 6 months
Falls self-efficacy
Activities Specific Balance Confidence Scale (ABC)
Measured: up to 6 months
Fall Efficacy
Self-report measurement tool: Falls Efficacy Scale (FES)
Measured: Up to 6 months
Fall catastrophization
Self-report of fall catastrophization: Catastrophization about Falls Questionnaire (CAFS)
Measured: Up to 6 months
Physical activity
Self-report measure physical activity: International Physical Activity Questionnaire (IPAQ)
Measured: Up to 6 months
Motor symptoms
Unified Parkinson's Disease Rating Scale motor subscale (UDPRS III)
Measured: Up to 6 months
Fear of falling
Self-report scale of avoidance behavior due to a fear of falling: Fear of Falls Avoidance Behavior Questionnaire (FFABQ)
Measured: Up to 6 months
Endurance
Endurance will be assessed using the 6 Minute Walk Test (6MWT).
Measured: Up to 6 months
bone health
Bone health will be measured using bone mineral densiometry (BMD).
Measured: up to 6 months
Mood
Mood will be measured using the Beck Depression Inventory.
Measured: up to 6 months
Catalase
Catalase concentrations from blood will be quantified utilizing enzyme-linked immunosorbent assays.
Measured: Up to 6 months
Cytokines
Cytokine (TNFα, IL-6, IL-10) concentrations from blood will be quantified utilizing enzyme-linked immunosorbent assays.
Measured: Up to 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Sep 2014 (estimated)
- Study startAug 2014
- Primary completionOct 2015
- Study completionDec 2015
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Parkinson's DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 27 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Nevada, Las Vegas
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Merrill Landers, University of Nevada, Las Vegas
- Investigators
- Merrill Landers, PT, DPT, PhD, Principal investigator, UNLV
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02230267
- Sponsor's protocol ID
- CTR-IN UNLVPT 2014.01
- Status last verified
- May 2016
- First submitted
- 27 Aug 2014
- Last updated
- 12 May 2016
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 12 May 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- High-intensity Exercise and Fall Prevention Boot Camp for Parkinson's Disease
- ClinicalTrials.gov ID
- NCT02230267
- Acronym / sponsor ID
- CTR-IN UNLVPT 2014.01
- Conditions
- Parkinson's Disease
- Keywords
- boot camp, exercise, balance training, fall prevention, falling, strength training
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 27 participants (actual)
- Lead sponsor
- University of Nevada, Las VegasUniversity, hospital or other
- Study start
- Aug 2014
- Primary completion
- Oct 2015 (actual)
- Study completion
- Dec 2015 (actual)
- First posted
- 3 Sep 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Several animal and human epidemiologic studies have provided evidence that exercise may be neuroprotective in Parkinson's disease (PD). Exercise may forestall diagnosis and, in the case of those who have already been diagnosed with PD, it may slow the observed neurodegeneration. Unfortunately, because this line of research is in early stages, there is little evidence to indicate what biological mechanisms underlie the neuroprotection that is conferred with exercise. Toward this end, it is possible that an interaction between endogenous antioxidant enzymes, inflammatory processes, and reactive oxygen species may be associated with exercise improvements in PD.
One of the most common reasons for premature death in PD is falls. Several meta-analyses have concluded that exercise training programs focused on balance and/or strength training are effective at improving aspects of balance. Taken together, the current body of evidence suggests that exercise may be neuroprotective and balance/strength training may decrease the likelihood of a fall. The combination of these efficacious treatment modalities (exercise and balance/strength training) in a comprehensive treatment approach to improve PD symptoms and balance has been previously reported at relatively mild or moderate exercise intensities. Because recent research has suggested that patients with PD may benefit more from more physically intense programs, we are proposing a more aggressive approach with regard to exercise intensity and frequency in the present trial. The primary purpose of this study is to determine the feasibility and safety of a high intensity exercise approach to PD. A secondary purpose is to determine the trajectory of change in outcomes over the duration of the trial from a high intensity fall prevention program. It is hoped that a signal of efficacy will allow this trial to progress to a comparative effectiveness trial. An important innovative design element is collecting biological assays to better understand the mechanism underlying the anticipated clinical improvements.
Aim 1 is to test the feasibility of a high-intensity exercise and fall prevention boot camp (HIBC) in patients with PD by analyzing adherence and whether they achieve minimum Centers for Disease Control exercise standards (150 min/wk moderate level aerobic exercise; strengthening at least two times per week) for the duration of the trial. Aim 2 is to determine if participation in an 8-week HIBC under the direction of a physical therapist is safe for individuals with PD. Secondary Aim 3 is to determine if participation in an 8-week HIBC will produce a signal of efficacy for several physical outcomes: falls per physical activity ratio, balance efficacy, motor activity, fatigue, muscle strength, bone health, cognition/mood, and quality of life. Secondary Aim 4 is to determine if participation in an 8-week HIBC will produce a signal of efficacy for biological outcomes, anti-inflammatory cytokines and anti-oxidant enzymes. An additional exploratory aim will be an analysis of BDNF val66val, val66met, met66met polymorphisms to determine if there is a differential response to exercise.
This trial is innovative because it utilizes a high intensity comprehensive exercise treatment approach (aerobic exercise, strengthening, and balance training). To our knowledge, there have been no trials of individuals with PD who have participated in a trial of this intensity in a group "boot camp" setting. Another innovative design element is the use of three novel assessments: biological assays of pro- and anti-inflammatory cytokines, endogenous anti-oxidant enzymes and a novel assessment of falls (falls per physical activity ratio).
Participants will be randomly assigned into either an 8-week HIBC group or an 8-week usual care control group (standard, low intensity group therapy class) under the direction of physical therapists. Each group will have 15 participants with a 1:5 patient-to-therapist ratio. The HIBC will be 1.5 hours daily, Monday through Friday. Participants will be required to attend 3 out of the 5 days. The protocol of the HIBC will include the following exercise components: A. 30 minutes of moderate-high intensity aerobic exercise; B. 15 minutes of strengthening the major muscle groups; C. 15 minutes of balance training; and, D. 15 minutes of interspersed rest and stretching. Participants will rotate through these four exercise components. Participants will have one baseline test and assessments at the 2-week, 4 week, 8-week, and 6-month points. Outcomes of the primary aims (Aim 1 and Aim 2) will be frequency counts of participation, adverse events, and compliance with exercise. The outcomes for the secondary aims will include measures of balance and falls, physical capacity, fatigue, exercise/physical activity behavior, and biological assays.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| High intensity boot camp | Experimental | Other: High intensity exercise and balance trainingEach of the two HIBCs will have 10 participants (20 total) with a 1:5 physical therapist-to-patient ratio. Each HIBC session will last 1.5 hours and will be held on 4 days of the week. Participants will be required to attend 3 of those 4 days but may attend all. Because this is a pragmatic trial, therapists will have some leeway to control the intensity and the modality of the exercise. However, the basic format of the HIBC will consist of the following exercise components: A. 30 minutes of moderate-high intensity aerobic exercise at 70%+ of estimated maximum heart rate; B. 15 minutes of strengthening the major muscle groups of the trunk and upper/lower extremities; C. 15 minutes of balance training; and, D. 15 minutes of rest and stretching. Participants will rotate through these four different exercise components in a circuit fashion. |
| Usual care arm | Active comparator | Other: Usual care arm exerciseThe low intensity exercise group will participate in the Fitness Counts Exercise Program (FCEP) which is a basic low intensity, sitting and standing exercise program (10 minutes of stretching, 10 minutes of aerobic exercise (60% of heart rate maximum), and 10 minutes of strengthening). This exercise program was developed by the National Parkinson Foundation and is commonly used in PD exercise classes. The physical therapist-to-patient ratio will be 1:5. As there are two clinical sites, there will be 10 participants in each of the two boot camps (20 total). The FCEP will be 1 hour daily on four days of the week. Participants will be required to attend 3 days per week but may attend more if they are able. |
Who may qualify
- Ages
- 45 to 85 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Neurologist-diagnosed idiopathic PD based on the UK PD brain bank criteria
- Aged 45-85
- Hoehn and Yahr stages 1-3 (mild to moderate PD)
- Participants do not anticipate a change in medication or surgical procedures in the next 8 months of the trial (2 months for the trial and 6 for the follow-up)
- Clearance from primary care physician to participate in the trial
Key exclusion criteria (6 listed)
- Poorly controlled or unstable cardiovascular disease that precludes participation in exercise
- Moderate-to-severe dementia using the Montreal Cognitive Assessment (MoCA). We will exclude participants with a MoCA cut off score of <26/30. This cut off value has excellent sensitivity (90%) and specificity (75%).
- Inability to stand or walk for more than 10 minutes
- Other significant disorders that would limit endurance exercise participation (i.e., osteoarthritis, stroke, respiratory problems, traumatic brain injury, neuromuscular disease, pain)
- Already participating in a regular, vigorous exercise program (3X/week or more of >60% estimated maximum heart rate)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| High intensity exercise and balance trainingAlso: A. 30 minutes of moderate-high intensity aerobic exercise at 70%+ of estimated maximum heart rate, B. 15 minutes of strengthening the major muscle groups of the trunk and upper/lower extremities, C. 15 minutes of balance training, D. 15 minutes of rest and stretching | Other | High intensity boot camp |
| Usual care arm exerciseAlso: 10 minutes of stretching, 10 minutes of aerobic exercise (60% of heart rate maximum), 10 minutes of strengthening | Other | Usual care arm |
Primary outcome
Frequency feasibility
Time frame: After completion of the 8 week trial
The number of participants that attend and participate in the treatment at least 3 times per week for 8 weeks.
Aerobic feasibility
Time frame: At the end of the 8 week trial
The number of participants that complete at least 150 minutes per week of moderate intensity exercise (70%+ of their estimated HR maximum). This will be ascertained using heart rate monitors.
Strength feasibility
Time frame: At the end of the 8 week trial
The number of participants that participate in strengthening exercises that incorporates all the major muscle groups at least two days per week.
Compliance
Time frame: At the end of the 8 week trial
Drop-out rate and reason for drop-out will be tracked.
Safety
Time frame: Ongoing throughout the 8 week trial
Exercise-related adverse events (e.g., strains/sprains, cardiovascular events).
Motivation
Time frame: At 8 weeks
The Intrinsic Motivation Inventory (IMI) will be used to gather information about motivation.
Falls
Time frame: At the end of the 8 week trial
Falls and fall injuries in and out of boot camp will be collected.
19 secondary outcomes
Falls
Time frame: up to 6 months
Motor activity
Time frame: up to 6 months
Fatigue
Time frame: up to 6 months
Strength
Time frame: up to 6 months
Cognition
Time frame: up to 6 months
Quality of life
Time frame: up to 6 months
Long term behavioral change
Time frame: up to 6 months
mini-Balance Evaluation Systems Test (mini-BESTest)
Time frame: up to 6 months
Falls self-efficacy
Time frame: up to 6 months
Fall Efficacy
Time frame: Up to 6 months
Fall catastrophization
Time frame: Up to 6 months
Physical activity
Time frame: Up to 6 months
Motor symptoms
Time frame: Up to 6 months
Fear of falling
Time frame: Up to 6 months
Endurance
Time frame: Up to 6 months
bone health
Time frame: up to 6 months
Mood
Time frame: up to 6 months
Catalase
Time frame: Up to 6 months
Cytokines
Time frame: Up to 6 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 May 2016.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Merrill Landers, PT, DPT, PhD principal investigator
UNLV
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing High intensity exercise and balance training in people with Parkinson's Disease, run by University of Nevada, Las Vegas at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 12 May 2016. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Frequency feasibility (time frame: After completion of the 8 week trial). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 May 2016.