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Completed

NCT Number: NCT01571258

Text4Diet: A Text Messaging Program for Weight Loss

The purpose of the present RCT is to evaluate a 12-month SMS intervention with expanded content, intervention strategies and interactive database logic, novel online enrollment, and automatic baseline scoring of measures to support a 12 month weight loss SMS intervention. The investigators hypothesized that the intervention group would have greater weight loss at 6 and 12 months than the control group and increased adherence to SMS would be associated with greater weight loss at 6 and 12 months.

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Key information

Age range

21 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Santech, Inc.

San Diego, California, 92121, United States

About this study

Background: Text messaging shows promise as an intervention mode for many health conditions due to its accessibility and timeliness . Few studies have evaluated the effectiveness of text message-based interventions for weight loss. This study is a randomized controlled trial comparing an intervention of daily text messaging (Text4Diet) focused on weight-related behaviors to a control group.

Participant Involvement: One hundred seventy overweight or obese adults will have their height and weight measured and complete a battery of questionnaires at baseline, 6 and 12 months. Participants in the intervention group will receive on average 4 texts per day consisting of weight related behavioral recommendations, knowledge based questions, and prompts to promote physical activity and weight monitoring. Texts are interactive and personally relevant based upon a baseline questionnaire. The control group will receive only monthly newsletters but not text messages. Participants in both conditions will receive monetary compensation for participation, travel to the study site, and reimbursements for text messaging.

Participants: Inclusion criteria consists of: a) age: 21 to 65 years, b) overweight or obese status: BMI between 25.0 and 39.9, c) regular access to the Internet, d) own and regularly use a cell phone and know how to use SMS, d) ability to read and speak English, and e) ability to participate in moderate PA. Exclusion criteria consists of a) current pregnancy or the intention of becoming pregnant during the 12 month trial, b) moving out of the country during the 12 month trial, and c) current eating disorder.

Dates: Recruitment for the RCT began in September 2010. The RCT began in January 2011 and ended in December 2011. Data analysis will occur through June 2012.

Location: San Diego, CA

Risks to Participants: This study involves low risk. Participation may involve some discomforts, such as embarrassment from sharing information about home environment, weight, and technology, diet, and exercise habits. There is a risk of loss of confidentiality of research information. All risks will be minimized according to the study protocol.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age: 21 to 65 years
  • overweight or obese status: BMI between 25.0 and 39.9
  • regular access to the Internet
  • own and regularly use a cell phone and know how to use SMS
  • ability to read and speak English
  • ability to participate in moderate PA.

Exclusion criteria

  • current pregnancy or the intention of becoming pregnant during the 12 month trial
  • moving out of the country during the 12 month trial
  • current eating disorder

Treatment and study plan

Text messaging

Behavioral

Participants in the intervention group will receive on average 4 texts per day consisting of weight related behavioral recommendations, knowledge based questions, and prompts to promote physical activity and weight monitoring. Texts are interactive and personally relevant based upon a baseline questionnaire.

Primary outcomes

  1. Weight

    Time frame: 6 months, 12 months

    We will assess the difference in weight loss between the intervention and the control group at 6 months and 12 months.

Secondary outcomes

  1. Pedometer Steps/Day

    Time frame: 6 months, 12 months

    Change in average pedometer steps per day in the intervention group.

  2. Adherence

    Time frame: 6 months, 12 months

    Level of adherence in responding to SMS. We also will investigate the correlation between adherence and weight loss.

  3. Treatment Satisfaction

    Time frame: 6 months and 12 months

    We will assess satisfaction with the SMS intervention in the intervention group only.

Sponsors and collaborators

Lead sponsor

Santech, Inc

Industry

Collaborators

  • National Cancer Institute (NCI)

Registry information

Acronym: Text4Diet

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Apr 5, 2012
Registry last updated
Apr 5, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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