Weight Loss and Healthy Diet Through Mobile Phone-enabled Social Interactions

NCT ID: NCT01957800

Last Updated: 2015-09-01

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

COMPLETED

Clinical Phase

NA

Total Enrollment

102 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-10-31

Study Completion Date

2014-11-30

Brief Summary

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A randomized controlled trial comparing the effects of the social-enabled internet weight loss and diet change intervention with the delayed treatment group for 3 months. We will study the effect of adding social interactions and supports to an Internet weight loss and diet change intervention. The website intervention will have action planning with social interactions and support features for sharing, reusing, recommending, and discussing strategies for improving habits. We hypothesize that the intervention group with access to the website will lose more weight than the delayed treatment group after three months.

Detailed Description

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Over the past two decades a very simple, low-cost and consistently effective intervention has been developed that we believe has potential to be disseminated online in primary care. The intervention, "action planning" (AP), is also known as "if-then planning" or "implementation intentions". Action Planning is one element of the process of self-regulation (Wing et al 2006; Luszczynska et al 2007), in which individuals identify (1) situations that challenge their ability to perform a behavior and (2) make a specific plan for what they will do when the situation is next encountered. Luszczynska and colleagues observed that adding a single session of action planning onto a portion-controlled meal intervention increased the weight lost from 2.1 kg to 4.2 kg (Luszczynska et al 2007). A meta-analysis of 94 studies using AP, nearly all of which included a single-dose, observed a mean effect size of Cohen's d=.65, consistent with a medium to large effect. Studies of repeated doses appear to have even greater effects (Chapman and Armitage 2010). Dr. Sciamanna recently completed a pilot feasibility study in which 53 subjects used an AP intervention for weight loss for 2 months. All subjects attended a 1-hour introductory session about the use of portion-controlled meals and pedometers. Subjects were then emailed one AP writing prompt each day, representing one of the 21 of the most common barriers to weight control (Bond et al 2001). Despite receiving no personalized feedback, over 2 months the subjects wrote action plans, on an average of 4.2 days per week. After 2 months, the average weight loss was 7.7 pounds. These adherence levels, though short-term, are greater than typical web-based weight control interventions included in a recent Cochrane review (Wieland 2012). This pilot study suggests that this low-cost intervention approach may have unusual levels of fidelity. Even though the average activities of user engagement with AP is quite high in the first two months, there is a slight decline toward the third month. In focus group discussions after a pilot conducted by Dr. Sciamanna in the Philadelphia area, participants of the pilot indicated consistent difficulties in coming up with ideas for habits that might be useful. These observations motivates this proposed study.

Conditions

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Overweight Obese

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Website

Group will be asked to complete a daily plan online for specific situations that tempt people to overeat. The website can be accessed online using a computer or smart phone and will allow participants to view others' plans. Participants will also be asked to enter their weight online every week.

Group Type EXPERIMENTAL

Website

Intervention Type BEHAVIORAL

Website will have action planning with social interactions and support features for sharing, reusing, and recommending strategies for improving habits.

Usual Care

Intervention Type BEHAVIORAL

Participants will record their weight and complete surveys online.

Usual Care

Group will be given access to the online intervention after the 3-month study ends.

Group Type ACTIVE_COMPARATOR

Usual Care

Intervention Type BEHAVIORAL

Participants will record their weight and complete surveys online.

Interventions

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Website

Website will have action planning with social interactions and support features for sharing, reusing, and recommending strategies for improving habits.

Intervention Type BEHAVIORAL

Usual Care

Participants will record their weight and complete surveys online.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Between 21-65 years old
* English speaking
* BMI from 27-50 kg/m2
* Access to the Internet at home or work for most days of the week
* Have current service for a smart phone with a camera and texting capability
* Able to use mobile phone to take a picture and send it to someone
* Able to use mobile phone to look for information on the internet using a search engine (such as Google)
* Able to use mobile phone to send and receive text messages
* Able to use mobile phone to send and receive emails
* Access to a scale at home

Exclusion Criteria

* Pregnant or planning to become pregnant in the next 3 months
* Planning on moving out of the area in the next 6 months
* Weigh more than 300 pounds
* Participating in an internet or community weight loss program
* Taking medication, prescription or over the counter for weight loss
* Doctor has said you have a heart condition and should only do physical activity recommended by a doctor
* Feel pain in chest when doing physical activity
* In the past month feel pain in chest when not doing physical activity
Minimum Eligible Age

21 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Penn State University

OTHER

Sponsor Role collaborator

Milton S. Hershey Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Christopher Sciamanna, MD, MPH

Professor of Medicine and Public Health Sciences; Division Chief of General Internal Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Christopher Sciamanna, MD, MPH

Role: PRINCIPAL_INVESTIGATOR

Milton S. Hershey Medical Center

Locations

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Penn State Milton S. Hershey Medical Center

Hershey, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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43474EP

Identifier Type: -

Identifier Source: org_study_id

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