AsthmaNCT02839252
Iggy and the Inhalers: A Study to Assess the Impact of an Asthma Education Program in School Age Children
A study testing Iggy and the Inhalers Asthma Education for Kids in people with Asthma, run by Wake Forest University Health Sciences at 1 site in United States.
Trial summary
The specific aims of this pilot study are to: 1. Evaluate the effectiveness of the asthma education intervention on asthma knowledge 2. Determine whether the asthma education intervention improves child and parent asthma treatment self-efficacy Our hypothesis is that the asthma education intervention will… Read more about this study
- Who is it for?
- Ages 8 to 12 years
- Conditions the study is for
- Asthma
- What is being tested?
- Iggy and the Inhalers Asthma Education for Kids
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 0 participants
- Where
- 1 siteUnited States
- Study dates
- Jul 2016to Jan 2018
- Phase
- Interventional
- 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 8 to 12 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Followed in the Yacktman General Pediatrics Clinic at Advocate Children's Hospital - Park Ridge (ACH-PR)
- Age 8 - 12 years
- Documented diagnosis of asthma (any severity level)
- Child and parent are English-speaking
- Child is currently taking an asthma medication on either a daily or an as-needed basis
- Parent permission/consent and child assent is obtained
Who cannot join
- Child has a diagnosis of another chronic lung or cardiovascular disease
- Child was assessed by parents or clinician to have a significant developmental delay, learning, or behavioral disability (e.g., autism spectrum)
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Iggy and the Inhalers: A Pilot Study to Assess the Impact of an Asthma Education Program in School Age Children
The specific aims of this pilot study are to:
- Evaluate the effectiveness of the asthma education intervention on asthma knowledge
- Determine whether the asthma education intervention improves child and parent asthma treatment self-efficacy
Our hypothesis is that the asthma education intervention will significantly improve asthma knowledge and asthma self-efficacy at 1 month post-intervention as compared to controls.
Read the detailed description
Potential subjects will be recruited from patients seen at Yacktman General Pediatrics Clinic. Investigators will initially use the clinic's electronic medical record (EMR) to identify potentially eligible subjects who have a regularly scheduled visit during the next 4 months. Once the patient is deemed eligible, they will be marked as "ASTHMA STUDY ELIGIBLE" in a red banner in the EMR. The parent will then be mailed a recruitment letter with parent permission/consent and child assent forms attached for their review. Once a potentially eligible patient shows up for a sick visit or a well visit, they will receive a handout reminding them of the study and asking them to consider participation. After their clinic visit, a designated pediatric resident will obtain parent permission/consent and child assent. Designated residents are those 2nd and 3rd year pediatric residents who have completed appropriate CITI training and financial conflict of interest disclosure, and have been trained by the PI on the study.
Study Endpoints:
The primary endpoint in this study is asthma knowledge at 2 time points: Immediately after the intervention (at the end of the initial clinic visit) and at 1-month post-intervention.
The secondary endpoint is asthma self-efficacy at the same 2 time points.
Procedures Involved:
This will be a prospective, randomized controlled clinical trial of an asthma educational intervention. It will compare two groups of children and their parents. One cohort will receive the asthma education intervention "Iggy and the Inhalers," and the other cohort will receive usual care in the outpatient, general pediatric clinic setting.
After recruitment procedures have been completed and the child and parent come into clinic for their scheduled visit, a member of the study team (designated resident or PI) will meet them and bring them to a specially designated room in the clinic. This process will occur after the patient's regularly scheduled visit. The study team member will then review the study, answer any questions, and obtain parent permission/consent and child assent. The study team member will indicate enrollment in the EMR by changing the banner to either "ASTHMA STUDY DECLINED" or "ASTHMA STUDY ENROLLED." For those who agree to participate, the parent and child will each be given 2 tools to complete:
- Parent:
- Asthma Knowledge: Parent Questionnaire
- Parent Asthma Self-efficacy survey
- Child:
- Asthma Knowledge: Child Questionnaire
- Child Self-efficacy Survey
In addition the parent will complete a demographic survey. While they are completing these tools, the study team member will determine the child's group assignment by consulting a random assignment log maintained at the clinic. Randomization will occur in blocks of 10 to allow equal group sizes for interim analyses. After the tools have been completed and collected, the child and parent will be informed of their group assignment, and study procedures will continue as follows.
Intervention Group:
After the baseline tools have been completed, the child will be given the Iggy Comic Book and trading cards. Parents and their children will then watch a 12-minute Iggy Video. At the completion of the video and prior to going home, the child and parent will complete the same 2 measures on asthma knowledge and self-efficacy. At 1-month after this clinic visit, the parent will be sent an email with a link to a Qualtrics survey that will contain a few supplemental questions to assess use of the intervention and the same 2 measures that the parent and the child completed at the initial visit. If we do not receive the completed surveys within 1-2 weeks, we will call them to remind them and offer them over the phone completion. If the parent asks to complete the online surveys they will again be given another 1-2 weeks. If the surveys are still not received, then we will make a 2nd call to repeat this process. If no success after this attempt, they will be deemed lost to follow-up. Once the surveys have been completed or the parent/child are deemed lost to follow up, the outpatient EMR banner will be changed to "ASTHMA STUDY COMPLETE." When the parent and child complete the final surveys, a thank you letter will be sent to the child and parent.
Control Group:
After the baseline tools have been completed, the parent and child will go home. At 1-month after the initial study clinic visit, the parent will be sent an email with a link to a Qualtrics survey that will contain a few supplemental questions to assess use of the intervention and the same 2 measures that the parent and the child completed at the initial visit. If the study team does not receive the completed surveys within 1-2 weeks, investigators will call them to remind them and offer them over the phone completion. If the parent asks to complete the online surveys the parents and children will again be given another 1-2 weeks. If the surveys are still not received, then investigators will make a 2nd call to repeat this process. If no success after this attempt, will be deemed lost to follow-up. Once the surveys have been completed or the parent/child are deemed lost to follow up, the outpatient EMR banner will be changed to "ASTHMA STUDY COMPLETE." When the parent and child complete the final surveys, the PI will send the control group a thank you letter with Iggy Comic Book, trading cards, and link to Iggy videos included.
Measures / Data Collection:
- Demographic Survey
- Includes: age, gender, ethnicity/race, primary language, residential zip code, education level of caregiver, annual household income, # of ED visits/hospitalizations for asthma symptoms over the past 1year. Baseline demographic information will be collected for each parent and child during the initial visit. These baseline measures include background information, which could become possible confounders for the study. This information is based on background information from similar studies published in this area.
- Asthma Knowledge Test Parent/Child
- Asthma knowledge will be assessed using 10-item multiple-choice questionnaires for both parents and children that was developed by Butz et al. Content was derived from the current National Asthma Educational Prevention Program (NAEPP) Guidelines, asthma symptom identification interventions, and was derived from a prior study on asthma education with the original authors permission. The child form was used in children 6-12 years of age. The final 10-item Asthma Knowledge Questionnaire reading level was written at a 4.7 grade level (Flesch-Kincaid grade level). Content validity of the parent and child knowledge scales, were assessed by an expert panel of pediatric allergists and general pediatricians, was high. Total scores on the asthma knowledge scale range from 0 to 10 points.
- Asthma Management Self-Efficacy Survey Parent/Child
- Self-efficacy will be assessed using a 13-question (Parent) and a 14-question (Child) survey. The survey utilizes a Likert scale response format and was designed to measure self-efficacy with regard to attack prevention and attack management. Acceptable to very good internal consistency reliabilities (Cronbach's alpha) were obtained for the final measures: Parent Asthma Self-Efficacy (alpha = 0.87) and Child Asthma Self-Efficacy (alpha = 0.87). The Parent Asthma Self-efficacy scale was positively correlated with parent ratings of their child's overall health, parent treatment efficacy, and child asthma self-efficacy. Child Asthma Self-efficacy was positively correlated with parent ratings of their children's health, Parent Asthma Self-Efficacy, Parent Treatment Efficacy, and the age of the child.
- Supplemental Questions to Assess Use of Intervention o These questions will allow us to assess the intervention dose. They will also provide feedback on the education program and allow it to be tailored to different pediatric populations.
Data to be recorded:
- Demographics (age, gender, ethnicity, primary language, residential zip code, education level of child and caregiver, household income, # of ED visits/hospitalizations for asthma symptoms over the past 1year)
- Asthma Knowledge Test Parent/Child: pre-, post-, and 1-month follow up scores
- Self Efficacy Survey Parent/Child: pre-, post-, 1-month follow up scores
- Responses to Supplemental Survey to Assess Use of the Intervention
- Comments on the program from parents and patients
- Conditions
- Asthma
- Being tested
- Iggy and the Inhalers Asthma Education for Kids
- Medical subject headings
- Asthma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Iggy and the Inhalers Asthma Education for KidsBehavioural
It is a comic book, trading cards, and stickers that teach kids about asthma. There is also a 12-minute cartoon video which teaches kids about asthma.
| Study group | Role | What they receive |
|---|---|---|
| Intervention Group | Experimental | After the baseline tools have been completed, the child will be given the Iggy Comic Book and trading cards. Parents and their children will then watch a 12-minute Iggy Video. At the completion of the video and prior to going home, the child and parent will complete the same 2 measures on asthma knowledge and self-efficacy. At 1-month after this clinic visit, the parent will be sent an email with a link to a Qualtrics survey that will contain a few supplemental questions to assess use of the intervention and the same 2 measures that the parent and the child completed at the initial visit. Receives: Behavioral: Iggy and the Inhalers Asthma Education for Kids |
| Control Group | No intervention | After the baseline tools have been completed, the parent and child will go home. At 1-month after the initial study clinic visit, the parent will be sent an email with a link to a Qualtrics survey that will contain a few supplemental questions to assess use of the intervention and the same 2 measures that the parent and the child completed at the initial visit. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Asthma knowledge
This will be measured by a 10 question multiple choice survey
Measured: Change in asthma knowledge immediately post-intervention and 1 month after intervention as compared with asthma knowledge prior to the intervention
Secondary outcomes (1)
Asthma Self Efficacy
This will be measured by a 14 question survey
Measured: Change in asthma self efficacy scores immediately post-intervention and 1 month after intervention as compared to pre-intervention self-efficacy scores
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Jul 2016 (estimated)
- Study startJul 2016
- Primary completionSep 2017 (estimated)
- Study completionJan 2018 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for AsthmaStudies of the same condition, open and under way.
- More trials run by Wake Forest University Health SciencesThe sponsor's other registered studies.
- 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 N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- Wake Forest University Health Sciences
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02839252
- Sponsor's protocol ID
- 6404
- Status last verified
- Feb 2018
- First submitted
- 15 Jul 2016
- Last updated
- 4 Oct 2024
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Oct 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Iggy and the Inhalers: A Pilot Study to Assess the Impact of an Asthma Education Program in School Age Children
- ClinicalTrials.gov ID
- NCT02839252
- Acronym / sponsor ID
- 6404
- Conditions
- Asthma
- Study type
- Interventional
- Recruitment status
- Withdrawn
- Enrolment
- 0 participants (actual)
- Lead sponsor
- Wake Forest University Health SciencesUniversity, hospital or other
- Study start
- Jul 2016
- Primary completion
- Sep 2017 (estimated)
- Study completion
- Jan 2018 (estimated)
- First posted
- 20 Jul 2016 (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.
The specific aims of this pilot study are to:
- Evaluate the effectiveness of the asthma education intervention on asthma knowledge
- Determine whether the asthma education intervention improves child and parent asthma treatment self-efficacy
Our hypothesis is that the asthma education intervention will significantly improve asthma knowledge and asthma self-efficacy at 1 month post-intervention as compared to controls.
Detailed description
Potential subjects will be recruited from patients seen at Yacktman General Pediatrics Clinic. Investigators will initially use the clinic's electronic medical record (EMR) to identify potentially eligible subjects who have a regularly scheduled visit during the next 4 months. Once the patient is deemed eligible, they will be marked as "ASTHMA STUDY ELIGIBLE" in a red banner in the EMR. The parent will then be mailed a recruitment letter with parent permission/consent and child assent forms attached for their review. Once a potentially eligible patient shows up for a sick visit or a well visit, they will receive a handout reminding them of the study and asking them to consider participation. After their clinic visit, a designated pediatric resident will obtain parent permission/consent and child assent. Designated residents are those 2nd and 3rd year pediatric residents who have completed appropriate CITI training and financial conflict of interest disclosure, and have been trained by the PI on the study.
Study Endpoints:
The primary endpoint in this study is asthma knowledge at 2 time points: Immediately after the intervention (at the end of the initial clinic visit) and at 1-month post-intervention.
The secondary endpoint is asthma self-efficacy at the same 2 time points.
Procedures Involved:
This will be a prospective, randomized controlled clinical trial of an asthma educational intervention. It will compare two groups of children and their parents. One cohort will receive the asthma education intervention "Iggy and the Inhalers," and the other cohort will receive usual care in the outpatient, general pediatric clinic setting.
After recruitment procedures have been completed and the child and parent come into clinic for their scheduled visit, a member of the study team (designated resident or PI) will meet them and bring them to a specially designated room in the clinic. This process will occur after the patient's regularly scheduled visit. The study team member will then review the study, answer any questions, and obtain parent permission/consent and child assent. The study team member will indicate enrollment in the EMR by changing the banner to either "ASTHMA STUDY DECLINED" or "ASTHMA STUDY ENROLLED." For those who agree to participate, the parent and child will each be given 2 tools to complete:
- Parent:
- Asthma Knowledge: Parent Questionnaire
- Parent Asthma Self-efficacy survey
- Child:
- Asthma Knowledge: Child Questionnaire
- Child Self-efficacy Survey
In addition the parent will complete a demographic survey. While they are completing these tools, the study team member will determine the child's group assignment by consulting a random assignment log maintained at the clinic. Randomization will occur in blocks of 10 to allow equal group sizes for interim analyses. After the tools have been completed and collected, the child and parent will be informed of their group assignment, and study procedures will continue as follows.
Intervention Group:
After the baseline tools have been completed, the child will be given the Iggy Comic Book and trading cards. Parents and their children will then watch a 12-minute Iggy Video. At the completion of the video and prior to going home, the child and parent will complete the same 2 measures on asthma knowledge and self-efficacy. At 1-month after this clinic visit, the parent will be sent an email with a link to a Qualtrics survey that will contain a few supplemental questions to assess use of the intervention and the same 2 measures that the parent and the child completed at the initial visit. If we do not receive the completed surveys within 1-2 weeks, we will call them to remind them and offer them over the phone completion. If the parent asks to complete the online surveys they will again be given another 1-2 weeks. If the surveys are still not received, then we will make a 2nd call to repeat this process. If no success after this attempt, they will be deemed lost to follow-up. Once the surveys have been completed or the parent/child are deemed lost to follow up, the outpatient EMR banner will be changed to "ASTHMA STUDY COMPLETE." When the parent and child complete the final surveys, a thank you letter will be sent to the child and parent.
Control Group:
After the baseline tools have been completed, the parent and child will go home. At 1-month after the initial study clinic visit, the parent will be sent an email with a link to a Qualtrics survey that will contain a few supplemental questions to assess use of the intervention and the same 2 measures that the parent and the child completed at the initial visit. If the study team does not receive the completed surveys within 1-2 weeks, investigators will call them to remind them and offer them over the phone completion. If the parent asks to complete the online surveys the parents and children will again be given another 1-2 weeks. If the surveys are still not received, then investigators will make a 2nd call to repeat this process. If no success after this attempt, will be deemed lost to follow-up. Once the surveys have been completed or the parent/child are deemed lost to follow up, the outpatient EMR banner will be changed to "ASTHMA STUDY COMPLETE." When the parent and child complete the final surveys, the PI will send the control group a thank you letter with Iggy Comic Book, trading cards, and link to Iggy videos included.
Measures / Data Collection:
- Demographic Survey
- Includes: age, gender, ethnicity/race, primary language, residential zip code, education level of caregiver, annual household income, # of ED visits/hospitalizations for asthma symptoms over the past 1year. Baseline demographic information will be collected for each parent and child during the initial visit. These baseline measures include background information, which could become possible confounders for the study. This information is based on background information from similar studies published in this area.
- Asthma Knowledge Test Parent/Child
- Asthma knowledge will be assessed using 10-item multiple-choice questionnaires for both parents and children that was developed by Butz et al. Content was derived from the current National Asthma Educational Prevention Program (NAEPP) Guidelines, asthma symptom identification interventions, and was derived from a prior study on asthma education with the original authors permission. The child form was used in children 6-12 years of age. The final 10-item Asthma Knowledge Questionnaire reading level was written at a 4.7 grade level (Flesch-Kincaid grade level). Content validity of the parent and child knowledge scales, were assessed by an expert panel of pediatric allergists and general pediatricians, was high. Total scores on the asthma knowledge scale range from 0 to 10 points.
- Asthma Management Self-Efficacy Survey Parent/Child
- Self-efficacy will be assessed using a 13-question (Parent) and a 14-question (Child) survey. The survey utilizes a Likert scale response format and was designed to measure self-efficacy with regard to attack prevention and attack management. Acceptable to very good internal consistency reliabilities (Cronbach's alpha) were obtained for the final measures: Parent Asthma Self-Efficacy (alpha = 0.87) and Child Asthma Self-Efficacy (alpha = 0.87). The Parent Asthma Self-efficacy scale was positively correlated with parent ratings of their child's overall health, parent treatment efficacy, and child asthma self-efficacy. Child Asthma Self-efficacy was positively correlated with parent ratings of their children's health, Parent Asthma Self-Efficacy, Parent Treatment Efficacy, and the age of the child.
- Supplemental Questions to Assess Use of Intervention o These questions will allow us to assess the intervention dose. They will also provide feedback on the education program and allow it to be tailored to different pediatric populations.
Data to be recorded:
- Demographics (age, gender, ethnicity, primary language, residential zip code, education level of child and caregiver, household income, # of ED visits/hospitalizations for asthma symptoms over the past 1year)
- Asthma Knowledge Test Parent/Child: pre-, post-, and 1-month follow up scores
- Self Efficacy Survey Parent/Child: pre-, post-, 1-month follow up scores
- Responses to Supplemental Survey to Assess Use of the Intervention
- Comments on the program from parents and patients
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Intervention Group | Experimental | Behavioral: Iggy and the Inhalers Asthma Education for KidsAfter the baseline tools have been completed, the child will be given the Iggy Comic Book and trading cards. Parents and their children will then watch a 12-minute Iggy Video. At the completion of the video and prior to going home, the child and parent will complete the same 2 measures on asthma knowledge and self-efficacy. At 1-month after this clinic visit, the parent will be sent an email with a link to a Qualtrics survey that will contain a few supplemental questions to assess use of the intervention and the same 2 measures that the parent and the child completed at the initial visit. |
| Control Group | No intervention | –After the baseline tools have been completed, the parent and child will go home. At 1-month after the initial study clinic visit, the parent will be sent an email with a link to a Qualtrics survey that will contain a few supplemental questions to assess use of the intervention and the same 2 measures that the parent and the child completed at the initial visit. |
Who may qualify
- Ages
- 8 to 12 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (6 listed)
- Followed in the Yacktman General Pediatrics Clinic at Advocate Children's Hospital - Park Ridge (ACH-PR)
- Age 8 - 12 years
- Documented diagnosis of asthma (any severity level)
- Child and parent are English-speaking
- Child is currently taking an asthma medication on either a daily or an as-needed basis
Key exclusion criteria (2 listed)
- Child has a diagnosis of another chronic lung or cardiovascular disease
- Child was assessed by parents or clinician to have a significant developmental delay, learning, or behavioral disability (e.g., autism spectrum)
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 |
|---|---|---|
| Iggy and the Inhalers Asthma Education for KidsIt is a comic book, trading cards, and stickers that teach kids about asthma. There is also a 12-minute cartoon video which teaches kids about asthma. | Behavioural | Intervention Group |
Primary outcome
Asthma knowledge
Time frame: Change in asthma knowledge immediately post-intervention and 1 month after intervention as compared with asthma knowledge prior to the intervention
This will be measured by a 10 question multiple choice survey
1 secondary outcome
Asthma Self Efficacy
Time frame: Change in asthma self efficacy scores immediately post-intervention and 1 month after intervention as compared to pre-intervention self-efficacy scores
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Oct 2024.
Related trials for Asthma
RecruitingPhase 1
Pilot Study to Identify the Mediators and Inflammatory Cell Surface Receptors Involved in Allergic Airway Inflammation
Asthma
RecruitingPhase 1
A Study to Compare the Relative Potency of Salbutamol Administered Via Metered Dose Inhalers (MDI) Containing Propellants HFA-152a to HFA-134a in Mild Asthmatics Aged 18 to 65 Inclusive
Asthma, Mild Asthma
RecruitingPhase 3
A Study Assessing the Effect of Dupilumab on Inducing Clinical Remission in Asthma
Asthma Control
Active, not recruitingPhase 2/3
Local Antibiotic Delivery for Community Acquired Pneumonia
Community Acquired Pneumonia (CAP)
RecruitingPhase 2
A Study to Learn About the Study Medicine Called PF-07275315 in People With Moderate-To-Severe Asthma
Asthma
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.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Iggy and the Inhalers Asthma Education for Kids in people with Asthma, run by Wake Forest University Health Sciences 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 2 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: withdrawn, as of the sponsor's last update on 4 Oct 2024. 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.
Are results available for this study?
The study was withdrawn before enrolling participants, so there are no results.
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?
Asthma knowledge (time frame: Change in asthma knowledge immediately post-intervention and 1 month after intervention as compared with asthma knowledge prior to the intervention). 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 4 Oct 2024.