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Improving Behavioral Weight Loss Via Electronic Handheld Device

Improving Behavioral Weight Loss Via Electronic Handheld Device

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01241578
Enrollment
20
Registered
2010-11-16
Start date
2010-02-28
Completion date
2012-06-30
Last updated
2015-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

Obesity, Behavior Therapy, Lifestyle, Technology, Cellular Phone

Brief summary

Standard behavioral treatment (SBT) for obesity is often effective, but weight losses are highly variable, and patients sometimes fail to achieve a successful weight loss of 5-10% of their starting weight. It has been suggested that the one size fits all approach of SBT may be responsible for many treatment failures because the intervention is not sufficiently tailored to address the unique needs of each patient. Moreover, treatment is delivered in the clinic, not in the settings and the times when it is needed most. The primary aim of the proposed research is to develop and pilot test a behavioral weight loss intervention that combines in-person sessions with treatment delivered via an electronic handheld device to provide highly individualized weight loss treatment in patients' natural environment. In a critical departure from previous research using cell phone technology, the portion of intervention that is delivered via handheld device will be of equal sophistication and importance to the portion of the intervention that is delivered in face-to-face treatment sessions. The proposed study seeks to determine the feasibility and preliminary efficacy of an individually tailored behavioral weight loss program that integrates clinic-based care and smartphone technology.

Interventions

BEHAVIORALLifestyle Counseling

Participants receive instructions for making healthy changes to their diet and physical activity habits.

Sponsors

The Obesity Society
CollaboratorOTHER
The Miriam Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Body Mass Index (kg/m2) of 30-45. * English language fluency * Basic familiarity with cell phone technology * Ability to read at a 6th grade level * Availability to attend weekly treatment sessions in Providence, RI

Exclusion criteria

* Any heart condition that limits ability to participate in physical activity * Chest Pain * Any cognitive of physical limitation that would preclude use of a smartphone * Serious mental illness * Historical or current eating disorder * Previous or planned bariatric surgery * Use of weight loss medication * Recent pregnancy or a plan to become pregnant in the next 6 months * Participation in a study at the Weight Control and Diabetes Research Center within the last two years * A weight loss of greater than 5% body weight in the last 6 months

Design outcomes

Primary

MeasureTime frameDescription
WeightBaseline and weekly for 24-weeks.Participants' body weight measured in kg.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026