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Study ID: NCT07224347. We help you review the study, but cannot decide medical eligibility.
Active Not RecruitingNCT07224347
Aspirin in Reducing Events in the Elderly-Extension (ASPREE-XT)
This study is active but not recruiting. It focuses on depression and currently lists study information in Australia and the United States.
Depression, Functional Disability, ...ObservationalOver 65 Years
The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.
Check recruitment and locations
Recruitment checked against the registry by HopeStage on . Registry information can change. Always confirm availability with the research team.
The overall study status can differ from each site's status. Open a country to see its locations and their registry status.
Australia · 14 sites
- Clinical Trials Unit, The Canberra HospitalGarran, Australian Capital TerritorySite status: Not listed — confirm with the team
- Illawarra Health and Medical Research Institute, University of WollongongWollongong, New South WalesSite status: Not listed — confirm with the team
- Discipline of General Practice, School of Population Health, University of AdelaideAdelaide, South AustraliaSite status: Not listed — confirm with the team
- Greater Green Triangle UniversityMount Gambier, South AustraliaSite status: Not listed — confirm with the team
- University of Tasmania Rural Clinical SchoolBurnie, TasmaniaSite status: Not listed — confirm with the team
- The Menzies Institute for Medical Research, University of TasmaniaHobart, TasmaniaSite status: Not listed — confirm with the team
- University of Tasmania Newnham CampusLaunceston, TasmaniaSite status: Not listed — confirm with the team
- Bendigo Regional Clinical SchoolBendigo, VictoriaSite status: Not listed — confirm with the team
- Geelong HospitalGeelong, VictoriaSite status: Not listed — confirm with the team
- Monash Mildura Regional Clinical SchoolMildura, VictoriaSite status: Not listed — confirm with the team
- University of BallaratMount Helen, VictoriaSite status: Not listed — confirm with the team
- Monash Gippsland Regional Clinical SchoolTraralgon, VictoriaSite status: Not listed — confirm with the team
- The South West Alliance of Rural Health (SWARH)Warrnambool, VictoriaSite status: Not listed — confirm with the team
- Gateway Community HealthWodonga, VictoriaSite status: Not listed — confirm with the team
United States · 22 sites
- The University of Alabama at BirminghamBirmingham, AlabamaSite status: Not listed — confirm with the team
- Howard UniversityWashington D.C., District of ColumbiaSite status: Not listed — confirm with the team
- Morehouse School of MedicineAtlanta, GeorgiaSite status: Not listed — confirm with the team
- Emory/ Atlanta VAMCAtlanta, GeorgiaSite status: Not listed — confirm with the team
- Rush Alzheimer's Disease CenterChicago, IllinoisSite status: Not listed — confirm with the team
- University of IowaIowa City, IowaSite status: Not listed — confirm with the team
- Pennington Biomedical Research CenterBaton Rouge, LouisianaSite status: Not listed — confirm with the team
- LSU Health Sciences- ShreveportShreveport, LouisianaSite status: Not listed — confirm with the team
- University of MichiganAnn Arbor, MichiganSite status: Not listed — confirm with the team
- Wayne State UniversityDetroit, MichiganSite status: Not listed — confirm with the team
- HealthPartners Research InstituteMinneapolis, MinnesotaSite status: Not listed — confirm with the team
- Phalen Village ClinicSaint Paul, MinnesotaSite status: Not listed — confirm with the team
- Wake Forest University Baptist Medical CenterGreensboro, North CarolinaSite status: Not listed — confirm with the team
- The Brody School of Medicine at East Carolina UniversityGreenville, North CarolinaSite status: Not listed — confirm with the team
- Einstein Medical CenterPhiladelphia, PennsylvaniaSite status: Not listed — confirm with the team
- University of Pittsburgh Health Sciences Research CenterPittsburgh, PennsylvaniaSite status: Not listed — confirm with the team
- Kent County Memorial HospitalPawtucket, Rhode IslandSite status: Not listed — confirm with the team
- University of Tennessee Health Science CenterMemphis, TennesseeSite status: Not listed — confirm with the team
- University of Texas Southwestern Medical Center at DallasDallas, TexasSite status: Not listed — confirm with the team
- University of Texas Medical BranchGalveston, TexasSite status: Not listed — confirm with the team
- Regional Academic Health CenterHarlingen, TexasSite status: Not listed — confirm with the team
- UT Health Science Center at San AntonioSan Antonio, TexasSite status: Not listed — confirm with the team
Key information made simple
What is this study testing?
This observational study follows adults living with depression to understand their experience, outcomes, or changes over time.
What would participation involve?
Participants may answer questionnaires, join interviews, or provide follow-up information, attend study visits with the research team. The registry lists locations in Australia and in the United States.
Who is it mainly for?
This study appears to be mainly for adults with depression.
What should you check before joining?
Ask about whether there is a comparison group, how many visits or travel steps are needed, the exact eligibility criteria.
Your next step
Study sites are listed in the registry. Recruitment status can differ between sites. Ask the research team to confirm the location, any in-person visits, time commitment, costs or compensation, and participation criteria.
Questions to ask before joining
- What are the exact eligibility criteria, and what could exclude someone?
- How many visits, assessments, or follow-ups are expected, and over what period?
- What risks, side effects, practical burdens, or alternatives should be understood first?
- Who should be contacted to confirm locations, timing, compensation, and next steps?
Things to check before joining
Study start dateStarted: July 15, 2019
- Recruitment status
- Active Not Recruiting
- Enrollment listed in the registry
- 19,114
- Sponsor
- Anne Murray
- Sponsor type
- Unknown or unclear
- Study type
- Observational
- Intervention type
- Interview / survey / observational
- Study phase
- Not clearly listed
- Locations
- United States, Australia
- Age range
- Over 65 Years
- Official registry ID
- NCT07224347
- Official title
- Aspirin in Reducing Events in the Elderly-Extension (ASPREE-XT)
- Official source
- Official registry link
Want help reviewing this study?
Study ID: NCT07224347. We help you review the study, but cannot decide medical eligibility.
For you
Participation may contribute to research. Personal benefit is not guaranteed.
Ask the research team to explain the activities, time commitment, and follow-up involved.
Study sites are listed. Confirm the relevant site and any travel before making plans.
Not medical advice
Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com
Questions about this study
What is this study trying to understand?
This study is exploring observational follow-up for people with depression. Participants may complete study visits, assessments, or follow-up activities defined by the research team. Direct benefit is not guaranteed. The detailed objective is not always clearly listed in the public registry; the study team can confirm.
Is this an interview, survey, or observational study?
This appears to be a interview / survey / observational study. Phase is mainly useful to check for medication studies and some device studies.
Who might this study be for?
This study may concern people with depression; age range: Over 65 Years. The criteria appear fairly broad, but you should not assume you are eligible. The study team must confirm diagnosis, age, exclusions, available locations, and next steps.
What would I likely need to do?
You may need to answer questionnaires or take part in interviews. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.
Could the questions feel emotionally difficult or personal?
If the study involves interviews or questionnaires, some questions may feel personal or emotionally sensitive. Ask whether you can skip questions, pause, stop, and how your answers will be protected. For any mental health study, also ask who to contact if you feel worse, whether participation may affect current treatment, whether you can stop, and who confirms eligibility.
Will I need to travel or attend in-person visits?
The listed study locations suggest that at least part of participation may involve a physical site. Ask which sites are open, how many visits are expected, whether any steps can be done remotely, and whether travel costs or compensation are listed.
Who is behind this study?
This study is sponsored by Anne Murray, which appears to be unknown or unclear. If available, it can be useful to check the sponsor website, collaborators, investigator affiliation, and the official registry before deciding. HopeStage does not judge the quality of a sponsor or researcher, but helps you identify what to verify.
Can I still join this study?
The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.
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