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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04051333
Other study ID # 2019P001649
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 30, 2020
Est. completion date December 31, 2021

Study information

Verified date February 2022
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is phase IIa feasibility and tolerability study of a mobile health (mHealth) application designed to study the effects of remote dietary counseling on disease progression and quality of life. The study will consist of two phases: Part I will consist of building and beta-testing the ALS Nutrition app and Part II will consist of enrolling a larger cohort of users into the app.


Description:

The investigators' prior work has shown that nutrition is an important modifiable prognostic factor for ALS disease progression and survival. In the recently completed E-Health Application To Measure Outcomes Remotely (EAT MORE) clinical trial (sponsored by the ALS Association), the investigators found that nutritional counseling supported by a mobile health (mHealth) app was associated with 0.5 points/month slower ALSFRS-R progression (p=0.17) and improved quality of life (p=0.09). The investigators are now designing an ALS-specific app that can be used by everyone with ALS, including those who do not live near ALS Centers. The app would help to address gaps in the delivery of ALS care by providing nutritional counseling, helping patients to manage and track their disease symptoms, and communicating with their providers. After the initial design has been tested by a group of NEALS patients and their caregivers, the study will advertise the app widely to recruit a larger group of ALS patients to measure nutrition and outcomes.


Recruitment information / eligibility

Status Completed
Enrollment 87
Est. completion date December 31, 2021
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Participants with a diagnosis of ALS (self-reported) 2. Male or female subjects aged 18 years or older. 3. Participants must be capable of providing informed consent and complying with trial procedures. 4. Participants must have access to an iOS or Android device to allow the to download the apps. Exclusion criteria: 1. Use of a feeding tube (G-tube or J-tube) 2. BMI>30 kg/m2 regardless of weight loss history 3. A history of cardiovascular disease (stroke, myocardial infarction, peripheral vascular disease) 4. A history of diabetes (self-reported)

Study Design


Related Conditions & MeSH terms


Intervention

Device:
ALS Nutrition App (MyDataHelps platform)
We have designed a mobile health app to provide nutritional counseling and to measure disease outcomes both through self-reported questionnaires and through passive data collection.

Locations

Country Name City State
United States Massachusetts General Hospital Boston Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Massachusetts General Hospital ALS Association

Country where clinical trial is conducted

United States, 

References & Publications (1)

Wills AM, Garry J, Hubbard J, Mezoian T, Breen CT, Ortiz-Miller C, Nalipinski P, Sullivan S, Berry JD, Cudkowicz M, Paganoni S, Chan J, Macklin EA. Nutritional counseling with or without mobile health technology: a randomized open-label standard-of-care-controlled trial in ALS. BMC Neurol. 2019 May 29;19(1):104. doi: 10.1186/s12883-019-1330-6. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Patient Reported Outcome Measurement Information System Short Form v1.0 Patient Reported Global Health Questionnaire where the higher the T score the better Change over time over 6 months
Secondary ALS Functional Rating Scale-Revised The ALSFRS-R total score ranges from 0-40 with higher scores better Change over time over 6 months
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