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

Sponsor
Eco Fusion (Industry)
Overall Status
Unknown status
CT.gov ID
NCT02621008
Collaborator
(none)
500
1
1
11
45.4

Study Details

Study Description

Brief Summary

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).

Condition or Disease Intervention/Treatment Phase
  • Other: Stress Reduction& Healthy living
N/A

Detailed Description

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
500 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Self-Administered Mobile Phone-based Holistic Intervention for Promoting Healthy Habits and Weight Loss in People Who Are Overweight or Obese
Study Start Date :
Nov 1, 2015
Anticipated Primary Completion Date :
Aug 1, 2016
Anticipated Study Completion Date :
Oct 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: 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.

Other: 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.

Outcome Measures

Primary Outcome Measures

  1. BMI [16 weeks]

  2. Glucose level [16 weeks]

  3. blood pressure [16 weeks]

  4. BMI [6 months]

  5. BMI [12 months]

  6. glucose level [6 months]

  7. glucose level [12 months]

  8. blood pressure [6 months]

  9. blood pressure [12 months]

Secondary Outcome Measures

  1. Quality of Life questionnaire [16 weeks]

  2. Quality of Life questionnaire [6 months]

  3. Quality of Life questionnaire [12 months]

  4. Burnout measure [16 weeks]

  5. Burnout Measure [6 months]

  6. Burnout measure [12 months]

  7. Perceived dietary adherence questionnaire [16 weeks]

  8. Perceived dietary adherence questionnaire [6 months]

  9. Perceived dietary adherence questionnaire [12 months]

  10. Mind wandering index [16 weeks]

    tendency and frequency of mind wandering

  11. Mind wandering index [6 months]

  12. Mind wandering index [1 year]

  13. stress mindset scale [16 weeks]

  14. stress mindset scale [6 months]

  15. stress mindset scale [1 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mt Sinai Medical Center New York New York United States 10029

Sponsors and Collaborators

  • Eco Fusion

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Eco Fusion
ClinicalTrials.gov Identifier:
NCT02621008
Other Study ID Numbers:
  • 007
First Posted:
Dec 3, 2015
Last Update Posted:
Jan 1, 2016
Last Verified:
Dec 1, 2015

Study Results

No Results Posted as of Jan 1, 2016