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NCT Number: NCT06821828

The Efficacy of Modified Olfactory Training for MCI High-Risk Individuals

The goal of this clinical trial is to validate the effectiveness of the modified olfactory training device, the main questions it aims to answer are: Is it possible that the device can delay the progression of MCI in older adults? Compared to the conventional device, how efficient is the modified olfactory training device for improving cognitive function?

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Key information

Age range

60 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Dawei Wu

Beijing, Beijing Municipality, 100191, China

Location contact

Dawei Wu, MD, PhD

CONTACT

[email protected]

+86 13522503401

Dawei Wu, MD, PhD

PRINCIPAL_INVESTIGATOR

About this study

Mild Cognitive Impairment (MCI) represents an intermediary stage between normal aging and dementia, with a significant proportion of cases progressing to dementia. No simple and effective therapeutic strategies are available to halt or reverse this progression. Olfactory dysfunction, a common early clinical manifestation of neurodegenerative diseases such as Alzheimer's Disease (AD), often precedes cognitive decline. Subjective Cognitive Decline (SCD) is increasingly recognized as a prodromal stage of MCI and dementia, which, together with olfactory dysfunction, provides a critical window for early intervention.

Conventional olfactory training (COT) has been shown to improve olfactory function, cognitive abilities, and brain connectivity in healthy elderly individuals, suggesting its potential to enhance neuroplasticity. Preliminary studies indicate that modified olfactory training (MOT) may yield superior outcomes compared to COT, with higher rates of olfactory recovery and improved deposition in the olfactory fissure. However, the efficacy of MOT in delaying or preventing the progression of olfactory dysfunction to MCI remains unclear.

In this study, the investigators planned to recruit 114 patients and divided them into three groups for control group and olfactory training with conventional and modified devices, and validate the effectiveness of the modified device based on changes in cognitive function and the comparison of the outcomes of the three groups.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age and Gender: Individuals aged 60-80 years, regardless of gender.
  • Diagnosis of Idiopathic Olfactory Dysfunction: overall TDI score below 30.75 points using the Sniffin' Sticks test. Without olfactory impairment due to traumatic, sinusitis-related, congenital, toxic/drug-induced causes, post-operative conditions, tumors, or post-upper respiratory infections.
  • Diagnosis of Subjective Cognitive Decline: Montreal Cognitive Assessment (MoCA) score >24 for middle school level and above, >19 for elementary school level, and >13 for illiterate individuals. Amyloid β (Aβ) deposition in the brain (defined as Aβ42 < 550 ∼ 813 pg/ml), the higher Formula of Hulstaert (defined as [(Aβ42/(240 + 1.18 × tau) ≤1]), and hippocampus atrophy.
  • Consent: Willingness to sign an informed consent form.

Exclusion criteria

  • Comorbid Chronic Diseases or Severe Concurrent Illnesses: Individuals with conditions such as hypertension, diabetes, bronchopneumonia, malignant tumors, or chronic obstructive pulmonary disease.
  • Recent Medication Use: Exclusion of participants who have taken corticosteroids, antimicrobials, leukotriene antagonists, or antihistamines within the last four weeks.
  • Inability to Comply with Study Requirements: Based on the researcher's judgment, individuals who are unable to tolerate olfactory function tests and treatment, complete the study or comply with its requirements due to memory or behavioral abnormalities, depression, severe alcohol consumption, or previous non-compliance.

Treatment and study plan

Modified olfactory training device

Combination Product

Participants will use a modified olfactory training device based on expiratory pressure. The advantages of the improved device are as follows: bi-directional airflow, positive pressure and the function of voice prompts and automatic counting.

Conventional olfactory training device

Combination Product

This device involves four brown glass jars (total volume 5 mL) with one of the four odors in each (1mL each, soaked in cotton pads to prevent spilling). The following odors were used: phenyl ethyl alcohol (PEA): rose, menthol: mint, citronellal: lemon, and eugenol: cloves. All jars were labeled with the odor name.

Primary outcomes

  1. Montreal Cognitive Assessment (MoCA) score

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    The MoCA score will be used to evaluate cognitive function across several domains including memory, attention, language, and orientation.

  2. Biomarkers of cognition (Blood/CSF)

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    This measure includes plasma and CSF levels of UGOT p-tau217, CSF Aβ42, p-tau181, total tau, and amyloid β 42 to total tau ratios. These biomarkers will help in assessing the biochemical progression of cognitive impairment.

  3. Neuroimaging assessments

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    This includes MRI scans focusing on temporal lobes and other brain regions, and amyloid PET scans to detect amyloid plaques. These imaging techniques will provide insights into structural and functional changes in the brain associated with cognitive decline.

  4. The Sniffin' Sticks test

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    a clinically significant olfactory improvement as measured by Sniffin' Sticks threshold, discrimination, and identification(TDI)( more than 6 scores)

Secondary outcomes

  1. Auditory Verbal Learning Test (AVLT)

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    Evaluates immediate memory recall, learning rate, and delayed recall, providing insights into verbal learning and memory.

  2. Digit Span Test (DST)

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    Assesses attention and working memory through forward and backward number recall tasks.

  3. Trail Making Test (TMT)

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    Measures visual attention and task switching by requiring participants to connect a sequence of numbers and letters as quickly as possible.

  4. Clock Drawing Test (CDT)

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    Used to assess visual-spatial abilities and executive function by having participants draw a clock showing a specific time.

  5. Boston Naming Test (BNT)

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    Measures language function, specifically object naming ability, which is crucial for everyday communication.

  6. Verbal Fluency Test (VFT)

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    Assesses cognitive flexibility and semantic memory by requiring participants to generate as many words as possible from a category in a limited time.

  7. Activities of Daily Living Scale (ADL)

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    Evaluates the participant's ability to perform everyday tasks independently, reflecting functional status.

  8. Instrumental Activities of Daily Living (IADL)

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    Assesses more complex daily living skills critical for independent living, such as managing finances and medication.

  9. Neuropsychiatric Inventory (NPI)

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    Measures behavioral changes including depression, anxiety, aggression, and apathy among others, providing a comprehensive overview of psychological status.

  10. Hamilton Anxiety Scale (HAMA)

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    Assesses the severity of anxiety symptoms, which can impact cognitive and daily functioning.

  11. Hamilton Depression Scale (HAMD)

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    Used to quantify the level of depressive symptoms, aiding in the assessment of mood disorders which can co-occur with cognitive decline.

  12. Olfactory bulb volume

    Time frame: Baseline,Month 3,Month 6,Month 12,Month 24

    Measurement of the olfactory bulb volume using MRI to assess changes or improvements in olfactory structures which might correlate with training efficacy.

Study contacts

Contact information is provided by the study sponsor or research team.

Dawei Wu

CONTACT

[email protected]

13522503401

Sponsors and collaborators

Lead sponsor

Peking University Third Hospital

Other

Collaborators

  • Peking University Sixth Hospital

Registry information

Official study title

Assessing Modified Olfactory Training to Prevent Cognitive Decline in MCI High-Risk Individuals: A Randomized Controlled Trial Protocol

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Feb 12, 2025
Registry last updated
Feb 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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