Mobile Phone-based Intervention for Promoting Healthy Habits and Weight Loss

NCT ID: NCT02621008

Last Updated: 2016-01-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

500 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-11-30

Study Completion Date

2016-10-31

Brief Summary

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A self administered 16 weeks plus follow up study to explore the efficacy of mobile phone driven apps for stress reduction coupled with guidance for healthy living among obese and overweight populations. The Study primary end points are weight of the participants, as well as glucose measurements (for subject with diabetes) and blood pressure (of subjects with hypertension).

Detailed Description

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The NewMe™ (Eco-fusion, Ltd) is a science driven lifestyle change program for better living (www.eco-fusion.com).

What's in the program? It starts with two weeks to shakeup the patient. It is focused on ridding the patient of known food addictions and helping the body patient return to its long forgotten normal operating environment. The patient is expected to notice a dramatic change in its well-being after those two weeks.

The NewMe program uses mobile health and motivational psychology to help impact sustainable lifestyle changes. The program takes a holistic approach to the etiology of adverse lifestyle habits and personalizes the solution to each individual. It is based on a variety of clinical constructs, including multiple studies related to biofeedback and stress relief, appended with the latest scientific development in nutrition and fitness, and enhanced with a technology platform specifically developed to deliver such care. The goal of the program is rapid and sustainable life changes with measurable parameters such as increased quality of life, reduced stress level, improved blood pressure and cholesterol, blood sugar and weight.

At the core of the system is a comprehensive clinical program combining nutrition, stress management, fitness, and social support, guided by a suite of software apps and emails which guide participants through a 16 weeks program, which is kick-started by a 2 weeks Rapid Start up Regimen. The solution combines a structured program and interactions and teaches participants how to integrate a healthier routine into their day-to-day life.

Core content include a broad behavioral focus on the principles of making healthy food choices and meal planning, instructions on how to combine both healthy diet and inclusion of an activity, stress \& sleep tracker. Stress gets special attention with the integration of breathing exercises, biofeedback training \& meditation into a daily routine in order to control and reduce emotional eating and other eating binges. This is done through the Serenita App.

To promote behavior change, the program introduces the cognitive and behavioral strategies, critical for long-term disease reversal. Other instructional content relates to the importance of including a modified high-nutrient density and fiber, low- caloric density foods in meal planning (although there is no caloric restriction in the program), managing self-defeating thinking patterns, and incorporating both fat burning \& strength training into a physical activity regime.

The program is divided into 2 stages:

* Stage One - Week 1 \& 2- Rapid Start up regimen, in which the participants follow a nutrient rich, low processed and carbs dietary regimen.
* In addition, using a personalized sensor driven app, participants practice daily breathing exercises \& guided meditation, intended to manage stress, and control food cravings. Physical activity regimen is also integrated into the daily routine. They confirm and log their daily activity which is software guided
* Stage two, weeks 3-16. During this period some of the restricted foods in Stage one are being reintroduced and the effect of reintroduction is explored.

Conditions

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Diabetes Hypertension Pre-diabetes Overweight Obese Weight Adherence

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Stress Reduction& Healthy living

Utilizing a stress reduction app (Serenita) and lifestyle intervention App (NewMe) and obtaining the NewMe guideline for healthy living, plus obtaining periodic messages regarding healthy living.

Group Type EXPERIMENTAL

Stress Reduction& Healthy living

Intervention Type OTHER

Utilizing a stress reduction app (Serenita) and lifestyle intervention App (NewMe) and obtaining the NewMe guideline for healthy living, plus obtaining periodic messages regarding healthy living.

Interventions

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Stress Reduction& Healthy living

Utilizing a stress reduction app (Serenita) and lifestyle intervention App (NewMe) and obtaining the NewMe guideline for healthy living, plus obtaining periodic messages regarding healthy living.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Be 18 years of age or older and
* have a body mass index (BMI) of at least 24 kg/m2 (22 kg/m2 if Asian) and
* be able to engage in light physical activity

Exclusion Criteria

* no Internet access or use of iOS
* taking more than three antihypertensive or diabetes drugs; meeting the DSM-5 criteria for an eating disorder
* having a disability that prevents or hinders exercise and physical activity
* receiving any treatment for weight loss elsewhere.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Eco Fusion

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Mt Sinai Medical Center

New York, New York, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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oren fuerst, ph.d.

Role: CONTACT

6466526531

Facility Contacts

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steven kaplan, md

Role: primary

646-652-6531

oren fuerst, phd

Role: backup

6466526531

Other Identifiers

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007

Identifier Type: -

Identifier Source: org_study_id

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