ClinicalTrials.gg
RecruitingNCT00233272Updated Nov 12, 2026

Baltimore Longitudinal Study of Aging

An observational study in Aging, sponsored by National Institute on Aging (NIA). Recruiting at 1 site in United States. Open to participants aged 20 Years to 120 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-12.

Sponsored by National Institute on Aging (NIA) · Observational

From the registry’s dates

  • Started Feb 2014; still recruiting 12 years 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
10,000
Ages
20 Years to 120 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 185 studies in Frailty with a site in United States — 50 open to participants now, 62 under way, 1 of them phase 3. Frailty · United States.

Planned enrollment
8th of 42
10,000 · median 128
Started
2014
with 5 others
Observational
42 of 185
10 open now
Registered
7th of 185
by date
Lead sponsor
6 of 185
National Institute on Aging (NIA)

Among the 185 studies in Frailty with a site in United States, this one is the 8th largest by planned enrollment of the 42 observational ones that give a count, is one of 6 that started in 2014, is one of 42 observational ones, and was the 7th registered.

Frailty

1,284 studies on the registry are indexed under Frailty; 451 are open to participants now.

Browse Frailty studies →

Open to participants now

50 of the 185 studies in Frailty with a site in United States are open now. Recruiting first, the newest first:

45 more — sign in →

All 50 open studies →

A study can be open while its sites in United States have not opened yet or have stopped. Only those recruiting at a site in United States →

Who these studies take

Of the 299 Frailty studies recruiting now, 235 (79%) set no upper age limit and 9 (3%) stop at 75 or younger; 7 take children under 18; 66 take healthy volunteers.

This study: 20 Years to 120 Years · all sexes · healthy volunteers too.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 185 studies in Frailty with a site in United States, or all of them as a file.
02

Study summary

Background:

- The Baltimore Longitudinal Study of Aging (BLSA) is a clinical research program on human aging that began in 1958. Volunteers of different ages join the study when they are healthy, and have follow-up visits for life. Visits last for multiple days. Participants are evaluated for many physical elements as well as for brain function. Physical tests are given. Information on mood, personality, and social aspects of life is also collected. This program has contributed more than any other research project to our understanding of aging.

Objectives:

- To characterize the many aspects of the aging process and learn how people can successfully adapt to aging.

Eligibility:

- Healthy individuals at least 20 years old.

Design:

  • Participants will receive a booklet and video describing the tests they will take.
  • During a 3-day visit at the study hospital, participants will take the following tests:
  • Urine will be collected for 24 hours. Blood samples will be taken. A small piece of muscle tissue may be collected by a needle.
  • A medical questionnaire and a physical exam will be given.
  • Participants hearts will be tested, including with blood pressure tests and electronic monitors. They will breathe into a tube to test their lungs.
  • Participants will perform several exercises, including treadmill walking.
  • Vision, hearing, and taste will be tested.
  • Bone and joint X-rays may be taken.
  • Imaging tests will be given, such as an MRI.
  • Participants will answer questions to test their mental abilities.
  • Participants will return for follow-up visits every few years for life. The tests listed above will be given at every visit.
Read the detailed description

The Baltimore Longitudinal Study of Aging (BLSA) is the NIA's major clinical research program in human aging that has been conducted in Baltimore since 1958. The study population is a series of healthy volunteers of different ages followed indefinitely with serial evaluations over time. The major aim of the study is to characterize the aging process in its multifaceted aspects. To accomplish this task, a large cohort of volunteers dispersed over a wide age range are enrolled in the study when they are healthy and then followed with regular follow-up visits for life. Since the aging process involves the whole range of physiological domains, participants receive an extensive evaluation of physiological parameters, biomarkers, risk factors, disease-related measures, impairments, and physical and cognitive function over follow-up visits that last for multiple days. Blood samples and other specimens are collected to obtain part of these measures and/or to be stored for future use. Information on mood, personality, psychological and social aspects of life that are relevant to the study of aging is also collected. Information collected in the BLSA represents a unique source of longitudinal data on aging. Historically the BLSA has contributed more than any other research project to our understanding of aging. More recently, the BLSA has begun to focus on factors associated with exceptionally healthy aging.

03

Conditions studied

  • Aging

Browse trials for

Keywords

  • Frailty
  • Disease Processes
  • Natural History
04

Who can participate

Ages eligible
20 Years to 120 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Healthy volunteers 20 years of age or older.

Eligibility criteria

  • INCLUSION CRITERIA:

These criteria pertain to the Screening Visit and Visit 1. If any of these conditions develop after this time, the participant remains in the study. In particular, participants who develop cognitive, motor or psychiatric conditions are retained in the study, although they are excluded from specific testing in which their underlying health condition is an exclusion criteria. Participants that refuse genetic testing and storage at Visit 1 will not be eligible to participate in the study.

  • Age greater than or equal to 20 years of age
  • Weigh less than or equal to 300lbs and/or (BMI) is less than or equal to 40
  • Do not have established genetic diseases
  • Are able to perform daily self- care without assistance
  • Are able to walk independently for at least 400 meters without assistance and without developing symptoms
  • Are able to perform normal activities of daily living without shortness of breath (walking or climbing stairs)
  • Do not have cognitive impairment based on screening tests and in the absence of any drug treatment
  • Do not have a history of cardiovascular disease (including angina, myocardial infarction, congestive heart failure, cerebrovascular diseases, uncontrolled hypertension)
  • Do not have a history of diabetes (requiring any medical treatment other than diet and exercise)
  • Do not have active (any activity in the last 10 years) cancer, except for locally limited basal or squamous cell cancer
  • Do not have hormonal dysfunction (Laboratory values out of range despite supplementation and/or drug treatment)
  • Do not have a history of neurological diseases or birth defects (other than minor anatomical abnormalities, which do not affect physical and/or cognitive function)
  • Do not have a history of kidney or liver disease (associated with reduced kidney or liver function)
  • Do not have a history of severe gastrointestinal (G.I.) diseases
  • Do not have muscle-skeletal conditions due to diseases or traumas (that cause pathological weakness and/or chronic pain)
  • Do not have a history of severe psychiatric conditions (associated with behavioral problems or requiring chronic medical treatment)
  • Do not have any medical condition that requires absolute and continuous need for long term treatment with antibiotics, , immunosuppressors, H2 blockers and/or proton pump inhibitors, or pain medications
  • Do not have important sensory deficits (legally blind and/or any condition that precludes the participant from being tested with standard neuropsychological tests or providing )
  • Able to read and speak English
  • Do not have joint replacements due to arthritic changes (joint replacements due to previous trauma are ok) or do not have 2 or more joint replacements for any reason
  • Do not meet any exclusionary criteria for 3T MRI and agrees to perform the test
  • Agree to genetic (DNA/RNA) sample collection, analysis, and storage at Visit 1

EXCLUSION CRITERIA:

These criteria pertain to the Screening Visit and Visit 1. If conditions considered as exclusion criteria for study entry develop any time after the this, the participant remains in the study.

Exclusion Criteria Based on Laboratory Assessment:

  • virus infection
  • or C
  • Syphilis
  • WBC > 12,000/mcrL
  • \< 100,000 or >600,000 /mcrL
  • \< 11 g/dL
  • Creatinine >1.5 mg/dl or calculated \< 50 cc/min
  • > 1.5 mg/dl (unless higher levels can be ascribed to Gilbert s disease)
  • , AST or alkaline phosphatase twice the normal serum concentration
  • Corrected calcium \< 8.5 or > 10.7 mg/dl
  • Albumin \< 3.1 g/dl
Terms in these criteria, in plain language(11)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

Creatinine clearance (CrCl)

How quickly the kidneys clear creatinine, a waste product, from the blood. A study may estimate it from a blood test with age, weight and sex (often by the Cockcroft–Gault formula), or measure it using blood and urine collected over a set time. Given in mL/min; higher is better.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
10,000 participants (estimated)

Groups and cohorts

  • Healthy Volunteers

    Healthy volunteers over a wide age-range

06

What researchers measure

Primary outcomes

  1. The major aim of the BLSA is to characterize the aging process in its multifaceted aspects.

    Characterization of the aging process

    Time frame: Ongoing

07

Study locations

1 of 1 sites recruiting
08

References and documents

Publications

  • Chia CW, Odetunde JO, Kim W, Carlson OD, Ferrucci L, Egan JM. GIP contributes to islet trihormonal abnormalities in type 2 diabetes. J Clin Endocrinol Metab. 2014 Jul;99(7):2477-85. doi: 10.1210/jc.2013-3994. Epub 2014 Apr 8. PubMed 24712564 ↗

Individual participant data

Plan to share: Undecided — There is ongoing discussion within the NIA IRP and a plan has not been finalized yet.

09

Timeline

1 registry update since Sep 25, 2026

Started Feb 2014 (actual).

How these figures are worked out, and which studies are left out of them.

Registered
Oct 3, 2005
First posted
Oct 5, 2005
StartActual
Feb 3, 2014
Last update
Nov 12, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Minor edits
Nothing that changes what the study is or who can join. Edited: verification date
1 update, last Nov 12, 2026
Show all 1 update
  1. Nov 12, 2026
    Minor edits only
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT00233272
Responsible party
Sponsor
First posted
Oct 5, 2005
Start date
Feb 3, 2014
Last update
Nov 12, 2026

Study contacts

Jeannie M Ruffolo, R.N.
Contact
ruffolojm@mail.nih.gov
(410) 350-7389
Luigi Ferrucci, M.D.
Contact
ferruccilu@grc.nia.nih.gov
(410) 558-8110
Luigi Ferrucci, M.D.
principal investigator · National Institute on Aging (NIA)

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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