Alzheimer Disease (AD)EXTRAGENIALNCT07385937
Effectiveness of Genistein in Mild Cognitive Impairment
A study testing Genistein in people with Alzheimer Disease (AD) and Mild Cognitive Impairment (MCI), run by Universidad Católica San Antonio de Murcia at 1 site in Spain.
Trial summary
Randomized, placebo-controlled, double-blind, multicenter clinical trial with two parallel study arms (experimental and placebo) to assess the efficacy of genistein extract consumption over 18 months on cognitive decline in patients with prodromal Alzheimer's disease. Read more about this study
- Who is it for?
- Ages 50 years and older
- Conditions the study is for
- Alzheimer Disease (AD), Mild Cognitive Impairment (MCI)
- What is being tested?
- Genistein
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 150 participants
- Where
- 1 siteSpain
- Study dates
- Feb 2026to Dec 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 50 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patient over 50 years of age.
- Patient diagnosed with mild cognitive impairment (MCI) for Alzheimer's disease (AD) according to the National Institute on Aging and Alzheimer's Association (NIA-AA, 2024) criteria:
- MMSE scores between 22 and 30 (inclusive; exceptions may be made for subjects with less than 5 years of education).
- Evidence of concern about change in cognition, compared to the person's previous level (subjective memory complaint/impairment for more than 6 months in the past year and/or confirmed by the informant and/or physician).
- A Clinical Dementia Rating (CDR) score of 0.5 with a memory domain score of 0.5.
- Essentially preserved activities of daily living.
- Evidence of elevated cortical amyloid by positron emission tomography (PET) with F18-flutemetamol. • Patients will be treated pharmaceutically according to the guidelines.
Who cannot join
- Diagnosis of a significant neurological disease other than Alzheimer's disease.
- Moderate depression as assessed by a Geriatric Depression Scale (GDS-D) score >8, or any other serious psychiatric disorder.
- Taking supplements containing isoflavones.
- Having a hormone-dependent neoplastic disease.
- Diagnosis of significant cerebrovascular disease.
- Having a serious systemic illness that would prevent completion of the study.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Spain1 site
UCAM HiTech, Sport & Health Innovation Hub
Murcia
Francisco Javier López Román, 968278157 ext. 157, jlroman@ucam.edu
About this study
Official title: Effectiveness of Genistein on the Progression of Cognitive Impairment in Patients With Mild Cognitive Impairment: Controlled Clinical Trial
Randomized, placebo-controlled, double-blind, multicenter clinical trial with two parallel study arms (experimental and placebo) to assess the efficacy of genistein extract consumption over 18 months on cognitive decline in patients with prodromal Alzheimer's disease.
Read the detailed description
The study aims to evaluate the effect of genistein over 18 months compared to placebo on the progression of cognitive impairment in subjects diagnosed with mild cognitive impairment (MCI) due to Alzheimer's disease (AD) in the following areas:
- Global assessment of dementia: overall evaluation of functionality and cognitive decline in MCI subjects.
- Global cognitive functions: assessment of general cognitive abilities.
- Episodic memory: evaluation of memory performance.
- Activities of daily living: assessment of the ability to perform basic and instrumental daily activities.
- Emotional and depressive state: evaluation of subjects' mood and depressive symptoms
- Being tested
- Genistein, Control product placebo
- Keywords
- Genistein, Dementia, Cognitive impairment, Neuroprotection, Prevention
- Medical subject headings
- Alzheimer Disease, Cognitive Dysfunction, Dementia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
GenisteinDietary supplement
Soy isoflavone
Control product placeboDietary supplement
It will be supplied in a color and shape similar to the active product, but with maltodextrin, an inert substance.
| Study group | Role | What they receive |
|---|---|---|
| Placebo | Placebo comparator | The product will have the same characteristics as the experimental product. Receives: Dietary Supplement: Control product placebo |
| Genistein | Experimental | Subjects will consume two capsules daily. Each capsule will be taken before the two main meals, each 100 mg tablet. Receives: Dietary Supplement: Genistein |
What is being measured
The primary outcome is the main question the study is designed to answer.
Cognitive function
The primary variable to be evaluated is the change in overall cognitive function and the deterioration in the ability to perform activities of daily living, assessed through the mean change by the Integrated Alzheimer's Disease Rating Scale (iADRS) score.
iADRS is an assessment tool designed to comprehensively measure cognitive and functional decline in patients with Alzheimer's disease, especially in the early stages. It combines elements of cognitive and functional assessment in a single scale, using ADAS-Cog and ADCS-ADL. In this case, version ADAS-Cog14 was used.
Measured: From baseline to month 18
Secondary outcomes (18)
Detection and assessment of cognitive impairment
The Mini-Mental State Examination (MMSE) is one of the most widely used tools for detecting and assessing cognitive impairment, including Alzheimer's disease. It is a brief and simple test that evaluates various cognitive functions: spatial and temporal orientation, immediate memory, attention and calculation, delayed memory, language, praxis (naming, repetition, comprehension of verbal commands, reading, spontaneous writing and copying drawings) and visual construction.
Measured: 18 months
Assess symptoms of depression
The GDS-15 (Geriatric Depression Scale - 15 items). This instrument was specifically designed for use in elderly populations to detect possible depression. It consists of 15 items with dichotomous yes/no responses.
Measured: 18 months
Severity of dementia
CDR-SB: A semi-structured interview with the primary informant and the patient, evaluated according to the evaluator's clinical judgment. It assesses the domains of Memory, Orientation, Judgment and Problem Solving, Community Affairs, Home and Hobbies, and Personal Care, with greater emphasis on the first domain.
Measured: 18 months
global cognition
ADAS-Cog: This test aims to measure the severity of dementia (global cognition, memory, language, etc.). The ADAS-Cog14 was chosen, which adds additional items (delayed word recall, digit cancellation, and maze or verbal fluency test) to the original test, improving the scale's sensitivity without significantly increasing assessment time.
Measured: 18 months
Assess functionality in patients with cognitive impairment
The ADCS-ADL and ADCS-ADL-MCI questionnaires assess functionality but they are aimed at different populations. ADCS-ADL aims to assess functionality in activities of daily living. ADCS-ADL-MCI, on the other hand, aims to assess the impact of Mild Cognitive Impairment (MCI) on Activities of Daily Living (ADLs).
Measured: 18 months
Activities of daily living
DAD-E: It aims to evaluate the functional impact of dementia on activities of daily living, through a questionnaire applied to the main informant.
Measured: 18 months
Assess verbal memory
The TAVEC (Test de Aprendizaje Verbal España-Complutense) is a neuropsychological tool widely used in Spain and other Spanish-speaking countries. It aims to assess episodic verbal memory, including learning, immediate recall, delayed recall, recognition, attention, and sensitivity to interference.
Measured: 18 months
Assess cognitive functions
The Trail Making Test (TMT) is a widely used neuropsychological test. It aims to assess processing speed, sustained and divided visual attention, visual tracking, executive functions (cognitive flexibility), and cognitive flexibility.
Measured: 18 months
visuospatial abilities and visual memory
The Clock Drawing Test (CDT) aims to evaluate visuospatial abilities and skills, visual memory and executive functions (strategy, organization).
Measured: 18 months
Assess visual memory, visuospatial perception, and executive functions
The Rey-Osterrieth Test is a widely used neuropsychological test for assessing visual memory, visuospatial perception, and executive functions. These functions are often affected in Alzheimer's disease, making this test useful in its assessment.
Measured: 18 months
Working memory and attention
Digit Span: It aims to assess short-term verbal memory (forward span) and auditory-verbal working memory (reverse span), as well as attention, sequencing, and mental manipulation of information.
Measured: 18 months
Ability to generate words within a specific category
Semantic fluency is a neuropsychological test. It aims to evaluate lexical-semantic access capacity, knowledge organization in memory, executive functions (planning, initiation, flexibility, response control), and semantic memory. This test is particularly useful for assessing executive function and language, two areas that are often affected in Alzheimer's disease.
Measured: 18 months
Assess executive functions
The F.A.B. (Frontal Assessment Battery) is a brief neuropsychological tool designed to assess executive functions, which are often affected in Alzheimer's disease and other dementias. It aims to evaluate executive functions (conceptualization, mental flexibility, motor programming, sensitivity to interference, inhibitory control, autonomy) by combining verbal instructions with tasks that require verbal responses or motor actions.
Measured: 18 months
Knowing the amount of ß-amyloid (βA) plaques
Positron emission tomography is a molecular imaging technique that measures the activity of a radiopharmaceutical that marks ß-amyloid (βA) plaques through the SUV (standard uptake value), which should be based on the amount of AB and can be relativized to match the change we expect to see. The mean change from baseline to month 18 in the standard uptake value (SUV) of composite cortical amyloid will be evaluated using the amyloid tracer [18F] flutemetamol by positron emission tomography (PET) imaging.
Measured: 18 months
Knowing the response to treatment
The inclusion of serum biomarkers may offer a more comprehensive perspective on the underlying mechanisms and response to treatment.
Measured: 18 months
Comorbidities and Medication
Take into account associated diseases, such as hypertension, diabetes, dyslipidemia, and other chronic diseases suffered by the patient, as well as concomitant medication. Document all medications that participants are taking at the start of the study or during its course, especially those that may influence cognitive function.
Measured: 18 months
Demographic variables
Age and gender; educational level; age and year of birth; tobacco and/or alcohol consumption.
Measured: 18 months
Safety
The safety of investigational products (IPs) will be assessed by recording adverse events (AEs) throughout the study, i.e., from the baseline visit to the final visit and a blood test.
Measured: 18 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Feb 2026
- Study startFeb 2026 (estimated)
- Primary completionJul 2027 (estimated)
- Study completionDec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Alzheimer Disease (AD)Studies 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
- Masking
- Triple blind
- Who is masked
- Participant, Care provider, Investigator
- Enrolment
- 150 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Universidad Católica San Antonio de Murcia
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Francisco Javier López Román, Universidad Católica San Antonio de Murcia
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07385937
- Sponsor's protocol ID
- UCAMCFE-00040
- Acronym
- EXTRAGENIAL
- Status last verified
- Feb 2026
- First submitted
- 26 Jan 2026
- Last updated
- 17 Feb 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 17 Feb 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effectiveness of Genistein on the Progression of Cognitive Impairment in Patients With Mild Cognitive Impairment: Controlled Clinical Trial
- ClinicalTrials.gov ID
- NCT07385937
- Acronym / sponsor ID
- EXTRAGENIAL / UCAMCFE-00040
- Keywords
- Genistein, Dementia, Cognitive impairment, Neuroprotection, Prevention
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 150 participants (estimated)
- Lead sponsor
- Universidad Católica San Antonio de MurciaUniversity, hospital or other
- Study start
- Feb 2026 (estimated)
- Primary completion
- Jul 2027 (estimated)
- Study completion
- Dec 2027 (estimated)
- First posted
- 4 Feb 2026 (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.
Randomized, placebo-controlled, double-blind, multicenter clinical trial with two parallel study arms (experimental and placebo) to assess the efficacy of genistein extract consumption over 18 months on cognitive decline in patients with prodromal Alzheimer's disease.
Detailed description
The study aims to evaluate the effect of genistein over 18 months compared to placebo on the progression of cognitive impairment in subjects diagnosed with mild cognitive impairment (MCI) due to Alzheimer's disease (AD) in the following areas:
- Global assessment of dementia: overall evaluation of functionality and cognitive decline in MCI subjects.
- Global cognitive functions: assessment of general cognitive abilities.
- Episodic memory: evaluation of memory performance.
- Activities of daily living: assessment of the ability to perform basic and instrumental daily activities.
- Emotional and depressive state: evaluation of subjects' mood and depressive symptoms
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, care provider, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Placebo | Placebo comparator | Dietary Supplement: Control product placeboThe product will have the same characteristics as the experimental product. |
| Genistein | Experimental | Dietary Supplement: GenisteinSubjects will consume two capsules daily. Each capsule will be taken before the two main meals, each 100 mg tablet. |
Who may qualify
- Ages
- 50 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- Patient over 50 years of age.
- Patient diagnosed with mild cognitive impairment (MCI) for Alzheimer's disease (AD) according to the National Institute on Aging and Alzheimer's Association (NIA-AA, 2024) criteria:
- Evidence of elevated cortical amyloid by positron emission tomography (PET) with F18-flutemetamol. • Patients will be treated pharmaceutically according to the guidelines.
Key exclusion criteria (6 listed)
- Diagnosis of a significant neurological disease other than Alzheimer's disease.
- Moderate depression as assessed by a Geriatric Depression Scale (GDS-D) score >8, or any other serious psychiatric disorder.
- Taking supplements containing isoflavones.
- Having a hormone-dependent neoplastic disease.
- Diagnosis of significant cerebrovascular disease.
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 |
|---|---|---|
| GenisteinSoy isoflavone | Dietary supplement | Genistein |
| Control product placeboIt will be supplied in a color and shape similar to the active product, but with maltodextrin, an inert substance. | Dietary supplement | Placebo |
Primary outcome
Cognitive function
Time frame: From baseline to month 18
The primary variable to be evaluated is the change in overall cognitive function and the deterioration in the ability to perform activities of daily living, assessed through the mean change by the Integrated Alzheimer's Disease Rating Scale (iADRS) score. iADRS is an assessment tool designed to comprehensively measure cognitive and functional decline in patients with Alzheimer's disease, especially in the early stages. It combines elements of cognitive and functional assessment in a single scale, using ADAS-Cog and ADCS-ADL. In this case, version ADAS-Cog14 was used.
18 secondary outcomes
Detection and assessment of cognitive impairment
Time frame: 18 months
Assess symptoms of depression
Time frame: 18 months
Severity of dementia
Time frame: 18 months
global cognition
Time frame: 18 months
Assess functionality in patients with cognitive impairment
Time frame: 18 months
Activities of daily living
Time frame: 18 months
Assess verbal memory
Time frame: 18 months
Assess cognitive functions
Time frame: 18 months
visuospatial abilities and visual memory
Time frame: 18 months
Assess visual memory, visuospatial perception, and executive functions
Time frame: 18 months
Working memory and attention
Time frame: 18 months
Ability to generate words within a specific category
Time frame: 18 months
Assess executive functions
Time frame: 18 months
Knowing the amount of ß-amyloid (βA) plaques
Time frame: 18 months
Knowing the response to treatment
Time frame: 18 months
Comorbidities and Medication
Time frame: 18 months
Demographic variables
Time frame: 18 months
Safety
Time frame: 18 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Feb 2026.
- Individual participant dataSharing planned: No
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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.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Genistein in people with Alzheimer Disease (AD) and Mild Cognitive Impairment (MCI), run by Universidad Católica San Antonio de Murcia at 1 site in Spain.
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 7 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: opening soon, as of the sponsor's last update on 17 Feb 2026. 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 Spain. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Francisco Javier López Román (968278157 ext. 157, jlroman@ucam.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Cognitive function (time frame: From baseline to month 18). 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 17 Feb 2026.