HIV PreventionSIIPANCT03278990
Scalable Interventions to Increase PrEP Adherence: Value Affirmation and Future Selves
A study testing Value Affirmation and Future Selves Combination in people with HIV Prevention, run by Stuart Fisk at 1 site in United States.
Trial summary
Pre-exposure prophylaxis, or PrEP, is a relatively new HIV prevention method where individuals who are at risk for HIV but do not currently have it take a daily pill (Truvada). PrEP has been proven medically effective and could help to reduce the rate of new HIV incidence in the United States, but in five large… Read more about this study
- Who is it for?
- Ages 18 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- HIV Prevention
- What is being tested?
- Value Affirmation and Future Selves Combination
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 26 participants
- Where
- 1 siteUnited States
- Study dates
- 19 Dec 2018to 16 Dec 2020
- 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 18 to 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- HIV- men and women, age 18 and higher, who are seeking PrEP and deemed appropriate per local site investigator following the CDC risk indication guidelines for PrEP.
- Must fit into one of the study's CDC-identified risk strata: a) IDUs and/or b) Caucasian LGBTQ or Minority LGBTQ
- Must be able to read and write English for themselves.
Who cannot join
- Same as that for PrEP initiation, e.g., existing HIV+ diagnosis or contra-indications, creatinine GFR < 60.
- Current or previous use of PrEP.
Trial locations and contacts
1 site in 1 country.
United States1 site
Center for Inclusion Health, Allegheny General Hospital
Pittsburgh, Pennsylvania, 15212
About this study
Official title: A Test of Scalable Behavioral Interventions to Increase PrEP Adherence for At-Risk HIV- Individuals: Value Affirmation and Future Selves
Pre-exposure prophylaxis, or PrEP, is a relatively new HIV prevention method where individuals who are at risk for HIV but do not currently have it take a daily pill (Truvada). PrEP has been proven medically effective and could help to reduce the rate of new HIV incidence in the United States, but in five large, randomized and controlled studies, many prospective PrEP patients chose not to take PrEP, and those that did often did not adhere to it consistently. How do we increase PrEP uptake and adherence amongst those most at risk for HIV? Also, will taking PrEP increase or decrease high-risk individual sexual behavior and HIV incidence? Here, the investigators propose a parallel group randomized, controlled clinical trial to test the effectiveness of a behavioral intervention designed to buffer individuals against stigma-related feelings, and to increase their connection to their selves twenty years in the future. The primary objective of the study is to increase PrEP adherence, as measured by the concentration of tenofovir diphosphate (TFV-DP) in dried blood spot samples (DBS). The secondary objectives are to decrease the incidence of STIs and increase safe sexual practices, as measured by clinic diagnoses and self-reported practices at 3, 6, 9 and 12 months.
This 12-month outpatient study will take place at four PrEP clinics in Pittsburgh and will enroll 170 subjects across 4 sites, with an expectation of retaining 80%, or 135 subjects. Eligibility includes male and female adults, ages 18-65, who are at risk of contracting HIV. Efforts will be made to recruit 33% of subjects from each of the following strata: 1) young, minority LGBT adults age 18-30 years of age; 2) Caucasian adults (MSM and heterosexual females) age 18-65 years of age; and 3) IDU adults, age 18-65, of any ethnic background.
Read the detailed description
Pre-exposure prophylaxis, or PrEP, is a relatively new HIV prevention method where individuals who are at risk for HIV but do not currently have it take a daily pill (Truvada). The CDC currently recommends PrEP as a method of HIV prevention in high-risk individuals based on compelling efficacy data from large international studies in diverse populations, but the issue of adherence and its relationship to clinical efficacy is still being defined. In five large, randomized and controlled studies, many prospective PrEP patients chose not to take PrEP, and those that did often did not adhere to it consistently (Landovitz \& Coates, 2014). Experts remain unable to answer several high-stakes questions: How do we increase PrEP uptake and adherence amongst those most at risk for HIV, and will starting PrEP increase or decrease high-risk individual sexual behavior and HIV incidence? (Landovitz \& Coates, 2014). In sum, the biggest challenge to reducing new HIV incidence in the U.S. is behavioral, not medical.
Here, the investigators propose a randomized, controlled clinical study to test the effectiveness of a "future selves-value affirmation" behavioral intervention on PrEP uptake and adherence. The intervention is designed to address the challenges of stigma and "present bias" - the individual propensity to place the gains of the moment ahead of future gains- as it relates to adherence.
"Present bias" and the suboptimal decisions it produces derive from a limited ability to imagine one's self in the future, and lead to a patient's preference for smaller, immediate rewards (e.g., escaping side effects of a medication, safeguarding one's situation from loved ones) over larger, delayed ones (e.g., not contracting HIV, longer life expectancy, better health). Research has shown that vivid, concrete, and detailed images of one's future self enhance a person's ability to envision and emotionally engage the future consequences of present-day decisions. For instance, creating positive images of one's future self has been shown to stem delinquent behavior for up to a year (van Gelder, 2013).
To address stigma, the investigators draw on another literature in psychology which has now established that short value affirmation exercises are able to enhance learning, performance, control and commitment outcomes, and to do so most effectively with populations facing stigma in the domain of interest (Vohs \& Smeichel, 2009; Creswell et al., 2013; Creswell \& Lindsay, 2014), especially within the domain of health behavior change (Ehret \& Sherman, 2014; Harris, 2011; Reed \& Aspinwall, 1998; Nustad, 2011; Cohen and Sherman, 2014; Epton et al., 2015). Affirmation exercises can be as simple as writing or talking for 5 minutes about a value one holds dear. Indeed, one such 5-minute exercise at the beginning of a new program or project can lead to profoundly powerful long-term outcomes across very different settings. For example, one intervention led to a .41 point grade increase for minority students in college over the course of one and two years (Cohen et al, 2009), increased decision making skills and use of public service information by homeless shelter participants in Seattle (Hall et al., 2014), and enabled smokers to more readily accept threatening smoking risk information (Epton et al., 2015). This study will combine value affirmation and future selves approaches.
The first study objective is to evaluate the effect of the "future-selves / value affirmation" intervention on PrEP adherence, as measured by tenofovir levels in dried blood spots and categorized via the 5-level ordinal measure for Engagement with PrEP (used in the iPrEx Open-Label Extension). The secondary study objectives are to evaluate the effect of the "future-selves / value affirmation" intervention on HIV and STI contraction at 3, 6, 9, and 12 months, and to evaluate the effect of the "future-selves / value affirmation" intervention on sexual risk behaviors, as self-reported numbers of anal/vaginal sex partners and episodes of condomless receptive anal and vaginal sex at 3, 6, 9 and 12 months.
This is a parallel group randomized trial with 2 arms-a control arm with allocation ratio of 50%, and an intervention arm (future self-value affirmation) with an allocation ratio of 50%. At each clinic visit, participants will engage in a 10-minute writing (or oral, for those with literacy challenges) exercises. Participants in the intervention arm will be given a list of values, asked to select one that has been particularly important to them at critical times in their life, then asked to write about why that value is important to them. Next, those same participants will write a letter to themselves twenty (20) years in the future. Participants in the control arm will first write for 5 minutes about why two values that are least important to them may be important to someone else, and next write a letter to themselves two weeks in the future.
The study includes 170 subjects enrolled across 4 sites in Pittsburgh, with an expectation of retaining 80%, or 135 subjects. Each subject's participation will last for 12 months.The entire study is expected to last for 18 months. The investigators will evaluate concentrations of tenofovir diphosphate (TFV-DP) in dried blood spot samples at baseline and then quarterly visits; they will also perform quarterly evaluations of self-reported numbers of anal/vaginal sex partners and episodes of condomless receptive anal and vaginal sex with and without condoms; incidence of STI and HIV acquisition.
The investigators will employ a mixed ANOVA to look at intervention effects on adherence-as well as STI incidence, and safe sex practices-across time intervals. They will also estimate mixed regression models for the intervention.
- Conditions
- HIV Prevention
- Being tested
- Value Affirmation and Future Selves Combination, Control writing exercise
- Keywords
- PrEP, Prevention, Value Affirmation, Future Selves, Behavioral Intervention
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Value Affirmation and Future Selves CombinationBehavioural
Following the questionnaire, participants will complete a 10- to 15-minute writing exercise. In the control condition, they will be given a list of values, select two that are least important to them, then write about why those values might be important to others. Next, they will write a short letter to themselves in 2 weeks. In the treatment condition, they will be given a list of values, select two that are important to them, then write for about why those values are important to them and how they have played a role in their life. They will then write a short letter to themselves twenty years in the future.
Control writing exerciseBehavioural
In this sham comparator, participants will also write, however, the content of the writing exercise is different. Participants write for five minutes about what they did that day. Next, for five minutes, they write a letter to themselves next week.
| Study group | Role | What they receive |
|---|---|---|
| Future Self - Value Affirmation | Experimental | This is a behavioral intervention whereby participants write (Value Affirmation and Future Selves Combination) for 5 minutes about 1-2 values that are important to them, as well as about a time in their life when they were particularly important. Next, for five minutes, they write a letter to themselves in 20 years. Receives: Behavioral: Value Affirmation and Future Selves Combination |
| Control | Sham comparator | In this sham comparator, participants will also write (Control Writing Exercise) --similar to the intervention above. However, the content of the writing exercise is different. Participants write for five minutes about what they did that day. Next, for five minutes, they write a letter to themselves next week. Receives: Behavioral: Control writing exercise |
What is being measured
The primary outcome is the main question the study is designed to answer.
PrEP Adherence
Tenofovir concentrations in dried blood spots
Measured: quarterly, for one year
Secondary outcomes (4)
HIV contraction
Diagnosis of HIV throughout the study period
Measured: quarterly, for one year
Sexual Risk Behavior 1: Partners
Number of Partners in anal or vaginal sex
Measured: quarterly, for one year
Sexual risk behavior 2: Condomless sex
number of condomless vaginal or anal sex occurrences
Measured: quarterly, for one year
STI contraction
Diagnosis of an STI throughout the study period
Measured: quarterly, for one year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Sep 2017
- Study start19 Dec 2018
- Primary completion16 Dec 2020
- Study completion16 Dec 2020
Why it stopped: Did not meet recruitment goals
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HIV PreventionStudies 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 N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- This is a parallel group randomized trial with 2 arms-a control arm with allocation ratio of 50%, and an intervention arm (future self-value affirmation) with an allocation ratio of 50%.
- Masking
- Double blind
- Who is masked
- Participant, Care provider
- Enrolment
- 26 participants (actual)
Sponsor and investigators
- Lead sponsor
- Stuart Fisk
- Sponsor type
- University, hospital or other
- Collaborators
- Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute), Gilead Sciences, University of Pittsburgh, Allies for Health + Wellbeing, Center for Inclusion Health, Allegheny General Hospital, Metro Community Health Center
- Responsible party
- Sponsor-investigator, Stuart Fisk, Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)
- Investigators
- Nichole Ben Itzhak, PhD, Study director, BI Development
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03278990
- Sponsor's protocol ID
- IN-US-276-4221
- Acronym
- SIIPA
- Status last verified
- Oct 2021
- First submitted
- 7 Sep 2017
- Last updated
- 11 Oct 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Only de-identified information will be shared regarding STI/HIV diagnosis.
Study at a glance
From the registry record, last updated by the sponsor on 11 Oct 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Test of Scalable Behavioral Interventions to Increase PrEP Adherence for At-Risk HIV- Individuals: Value Affirmation and Future Selves
- ClinicalTrials.gov ID
- NCT03278990
- Acronym / sponsor ID
- SIIPA / IN-US-276-4221
- Conditions
- HIV Prevention
- Keywords
- PrEP, Prevention, Value Affirmation, Future Selves, Behavioral Intervention
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Did not meet recruitment goals
- Enrolment
- 26 participants (actual)
- Lead sponsor
- Stuart FiskUniversity, hospital or other
- Collaborators
- Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute), Gilead Sciences, University of Pittsburgh, Allies for Health + Wellbeing, Center for Inclusion Health, Allegheny General Hospital, Metro Community Health Center
- Study start
- 19 Dec 2018 (actual)
- Primary completion
- 16 Dec 2020 (actual)
- Study completion
- 16 Dec 2020 (actual)
- First posted
- 12 Sep 2017 (actual)
- 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.
Pre-exposure prophylaxis, or PrEP, is a relatively new HIV prevention method where individuals who are at risk for HIV but do not currently have it take a daily pill (Truvada). PrEP has been proven medically effective and could help to reduce the rate of new HIV incidence in the United States, but in five large, randomized and controlled studies, many prospective PrEP patients chose not to take PrEP, and those that did often did not adhere to it consistently. How do we increase PrEP uptake and adherence amongst those most at risk for HIV? Also, will taking PrEP increase or decrease high-risk individual sexual behavior and HIV incidence? Here, the investigators propose a parallel group randomized, controlled clinical trial to test the effectiveness of a behavioral intervention designed to buffer individuals against stigma-related feelings, and to increase their connection to their selves twenty years in the future. The primary objective of the study is to increase PrEP adherence, as measured by the concentration of tenofovir diphosphate (TFV-DP) in dried blood spot samples (DBS). The secondary objectives are to decrease the incidence of STIs and increase safe sexual practices, as measured by clinic diagnoses and self-reported practices at 3, 6, 9 and 12 months.
This 12-month outpatient study will take place at four PrEP clinics in Pittsburgh and will enroll 170 subjects across 4 sites, with an expectation of retaining 80%, or 135 subjects. Eligibility includes male and female adults, ages 18-65, who are at risk of contracting HIV. Efforts will be made to recruit 33% of subjects from each of the following strata: 1) young, minority LGBT adults age 18-30 years of age; 2) Caucasian adults (MSM and heterosexual females) age 18-65 years of age; and 3) IDU adults, age 18-65, of any ethnic background.
Detailed description
Pre-exposure prophylaxis, or PrEP, is a relatively new HIV prevention method where individuals who are at risk for HIV but do not currently have it take a daily pill (Truvada). The CDC currently recommends PrEP as a method of HIV prevention in high-risk individuals based on compelling efficacy data from large international studies in diverse populations, but the issue of adherence and its relationship to clinical efficacy is still being defined. In five large, randomized and controlled studies, many prospective PrEP patients chose not to take PrEP, and those that did often did not adhere to it consistently (Landovitz \& Coates, 2014). Experts remain unable to answer several high-stakes questions: How do we increase PrEP uptake and adherence amongst those most at risk for HIV, and will starting PrEP increase or decrease high-risk individual sexual behavior and HIV incidence? (Landovitz \& Coates, 2014). In sum, the biggest challenge to reducing new HIV incidence in the U.S. is behavioral, not medical.
Here, the investigators propose a randomized, controlled clinical study to test the effectiveness of a "future selves-value affirmation" behavioral intervention on PrEP uptake and adherence. The intervention is designed to address the challenges of stigma and "present bias" - the individual propensity to place the gains of the moment ahead of future gains- as it relates to adherence.
"Present bias" and the suboptimal decisions it produces derive from a limited ability to imagine one's self in the future, and lead to a patient's preference for smaller, immediate rewards (e.g., escaping side effects of a medication, safeguarding one's situation from loved ones) over larger, delayed ones (e.g., not contracting HIV, longer life expectancy, better health). Research has shown that vivid, concrete, and detailed images of one's future self enhance a person's ability to envision and emotionally engage the future consequences of present-day decisions. For instance, creating positive images of one's future self has been shown to stem delinquent behavior for up to a year (van Gelder, 2013).
To address stigma, the investigators draw on another literature in psychology which has now established that short value affirmation exercises are able to enhance learning, performance, control and commitment outcomes, and to do so most effectively with populations facing stigma in the domain of interest (Vohs \& Smeichel, 2009; Creswell et al., 2013; Creswell \& Lindsay, 2014), especially within the domain of health behavior change (Ehret \& Sherman, 2014; Harris, 2011; Reed \& Aspinwall, 1998; Nustad, 2011; Cohen and Sherman, 2014; Epton et al., 2015). Affirmation exercises can be as simple as writing or talking for 5 minutes about a value one holds dear. Indeed, one such 5-minute exercise at the beginning of a new program or project can lead to profoundly powerful long-term outcomes across very different settings. For example, one intervention led to a .41 point grade increase for minority students in college over the course of one and two years (Cohen et al, 2009), increased decision making skills and use of public service information by homeless shelter participants in Seattle (Hall et al., 2014), and enabled smokers to more readily accept threatening smoking risk information (Epton et al., 2015). This study will combine value affirmation and future selves approaches.
The first study objective is to evaluate the effect of the "future-selves / value affirmation" intervention on PrEP adherence, as measured by tenofovir levels in dried blood spots and categorized via the 5-level ordinal measure for Engagement with PrEP (used in the iPrEx Open-Label Extension). The secondary study objectives are to evaluate the effect of the "future-selves / value affirmation" intervention on HIV and STI contraction at 3, 6, 9, and 12 months, and to evaluate the effect of the "future-selves / value affirmation" intervention on sexual risk behaviors, as self-reported numbers of anal/vaginal sex partners and episodes of condomless receptive anal and vaginal sex at 3, 6, 9 and 12 months.
This is a parallel group randomized trial with 2 arms-a control arm with allocation ratio of 50%, and an intervention arm (future self-value affirmation) with an allocation ratio of 50%. At each clinic visit, participants will engage in a 10-minute writing (or oral, for those with literacy challenges) exercises. Participants in the intervention arm will be given a list of values, asked to select one that has been particularly important to them at critical times in their life, then asked to write about why that value is important to them. Next, those same participants will write a letter to themselves twenty (20) years in the future. Participants in the control arm will first write for 5 minutes about why two values that are least important to them may be important to someone else, and next write a letter to themselves two weeks in the future.
The study includes 170 subjects enrolled across 4 sites in Pittsburgh, with an expectation of retaining 80%, or 135 subjects. Each subject's participation will last for 12 months.The entire study is expected to last for 18 months. The investigators will evaluate concentrations of tenofovir diphosphate (TFV-DP) in dried blood spot samples at baseline and then quarterly visits; they will also perform quarterly evaluations of self-reported numbers of anal/vaginal sex partners and episodes of condomless receptive anal and vaginal sex with and without condoms; incidence of STI and HIV acquisition.
The investigators will employ a mixed ANOVA to look at intervention effects on adherence-as well as STI incidence, and safe sex practices-across time intervals. They will also estimate mixed regression models for the intervention.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, care provider)
- Number of arms
- 2
- Model description
- This is a parallel group randomized trial with 2 arms-a control arm with allocation ratio of 50%, and an intervention arm (future self-value affirmation) with an allocation ratio of 50%.
| Arm | Type | Receives |
|---|---|---|
| Future Self - Value Affirmation | Experimental | Behavioral: Value Affirmation and Future Selves CombinationThis is a behavioral intervention whereby participants write (Value Affirmation and Future Selves Combination) for 5 minutes about 1-2 values that are important to them, as well as about a time in their life when they were particularly important. Next, for five minutes, they write a letter to themselves in 20 years. |
| Control | Sham comparator | Behavioral: Control writing exerciseIn this sham comparator, participants will also write (Control Writing Exercise) --similar to the intervention above. However, the content of the writing exercise is different. Participants write for five minutes about what they did that day. Next, for five minutes, they write a letter to themselves next week. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- HIV- men and women, age 18 and higher, who are seeking PrEP and deemed appropriate per local site investigator following the CDC risk indication guidelines for PrEP.
- Must fit into one of the study's CDC-identified risk strata: a) IDUs and/or b) Caucasian LGBTQ or Minority LGBTQ
- Must be able to read and write English for themselves.
Key exclusion criteria (2 listed)
- Same as that for PrEP initiation, e.g., existing HIV+ diagnosis or contra-indications, creatinine GFR < 60.
- Current or previous use of PrEP.
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 |
|---|---|---|
| Value Affirmation and Future Selves CombinationFollowing the questionnaire, participants will complete a 10- to 15-minute writing exercise. In the control condition, they will be given a list of values, select two that are least important to them, then write about why those values might be important to others. Next, they will write a short letter to themselves in 2 weeks. In the treatment condition, they will be given a list of values, select two that are important to them, then write for about why those values are important to them and how they have played a role in their life. They will then write a short letter to themselves twenty years in the future. | Behavioural | Future Self - Value Affirmation |
| Control writing exerciseIn this sham comparator, participants will also write, however, the content of the writing exercise is different. Participants write for five minutes about what they did that day. Next, for five minutes, they write a letter to themselves next week. | Behavioural | Control |
Primary outcome
PrEP Adherence
Time frame: quarterly, for one year
Tenofovir concentrations in dried blood spots
4 secondary outcomes
HIV contraction
Time frame: quarterly, for one year
Sexual Risk Behavior 1: Partners
Time frame: quarterly, for one year
Sexual risk behavior 2: Condomless sex
Time frame: quarterly, for one year
STI contraction
Time frame: quarterly, for one year
Results and safety
The study was stopped early (reason given: Did not meet recruitment goals). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Oct 2021.
- Individual participant dataSharing planned: No. Only de-identified information will be shared regarding STI/HIV diagnosis.
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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.
Nichole Ben Itzhak, PhD study director
BI Development
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Value Affirmation and Future Selves Combination in people with HIV Prevention, run by Stuart Fisk 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 3 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: stopped early, as of the sponsor's last update on 11 Oct 2021. 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. Some participants in this study may receive a placebo. 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 stopped early (reason given: Did not meet recruitment goals). Results are not available in the source record.
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?
PrEP Adherence (time frame: quarterly, for one year). 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 11 Oct 2021.