CClinicalTrials.gg
Status unknownNCT03702543Updated Oct 11, 2018

Managing Vascular Dementia Risk Factors With SymTrend

A Phase 1 interventional study of SymTrend, Inc. in Vascular Dementia, sponsored by SymTrend Inc.. Status unknown at 1 site in United States. Open to participants aged 30 Years and older. Per ClinicalTrials.gov, last updated 2018-10-11.

Sponsored by SymTrend Inc. · Phase 1, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Oct 2018), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 1
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Ages
30 Years and older
Sex
All
01

Study summary

Individuals with uncontrolled vascular disease are at risk for an insidious progression of brain injury starting in early to midlife and ultimately culminating in a vascular dementia, robbing them of activities of daily living independence. Successful containment of this progression requires rigorous vascular risk factor management - the control of blood pressure, blood sugars, weight, and alcohol consumption; the cessation of smoking, and an increase in aerobic activity. SymTrend's mobile and web system for managing vascular risk factors will help improve adherence to health and lifestyle strategies, will stem cognitive decline, and will preserve independence in the community for older adults.

Read the detailed description

Neurologists from Massachusetts General Hospital will refer 10 adults with vascular mild cognitive impairment for participation in this project. The patients will be given Bluetooth devices appropriate for their condition and will be trained to use SymTrend and Apple Health software. They will use the software and devices for three months; will receive messages throughout from the system and/or a research coordinator about their progress, with encouragement and strategies to fully manage their symptoms; and their neurologist will be in communication with them about the progress charts and will adjust their care on the basis of this real-time data.

02

Conditions studied

  • Vascular Dementia
03

In context

Dementia

2,172 studies on the registry are indexed under Dementia; 540 are open to participants now.

This study's planned enrollment of 10 is below the median of 83 across 1,629 interventional studies indexed under Dementia.

Browse Dementia studies →

Lead sponsor

SymTrend Inc. is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Prior incidence of neurological event such as transient ischemic attack, stroke.

Exclusion criteria

Exclusion Criteria:

  • Inability to use smartphone,
  • Inability to read English
05

Study design

Phase
Phase 1
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
10 participants (estimated)

Interventions

  • BehavioralSymTrend, Inc.

    Use of SymTrend and Apple Health apps with feedback and strategies provided.

06

What researchers measure

Primary outcomes

  1. Improved management of blood sugar

    Blood sugars are measured regularly and are maintained within bounds prescribed by MD

    Time frame: three months

  2. Improved blood pressure management

    Blood pressure is measured regularly and is within bounds prescribed by MD

    Time frame: three months

  3. Reduced smoking

    Number of cigarettes smoked is reduced or eliminated

    Time frame: three months

  4. Weight is reduced if necessary

    Food intake is reduced and is healthier, and as a consequence weight is reduced

    Time frame: three months

  5. Activity level is increased

    Step count increases continuously throughout study period

    Time frame: three months

Secondary outcomes

  1. Fatigue is reduced if originally is a problem

    Hours sleep increases and frequency of sleep interruption reduces

    Time frame: three months

07

Study locations

1 site
  • Neurology Department, Massachusetts General Hospital
    Boston, Massachusetts 02114, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 11, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03702543
Lead sponsor
SymTrend Inc.
Collaborators
National Institute on Aging (NIA), Massachusetts General Hospital
Responsible party
Sponsor
First posted
Oct 11, 2018
Start date
Oct 15, 2018 (estimated)
Primary completion
Oct 14, 2019 (estimated)
Completion
Oct 14, 2019 (estimated)
Last update
Oct 11, 2018

Study contacts

Minna Levine, Phd
Contact
symtrend@gmail.com
16174917510
Minna Levine, Phd
principal investigator · SymTrend Inc.

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2018. You cannot join it, but the record below documents what was studied.

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