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Using a State-wide Initiative to Disseminate Effective Behavioral Weight Loss Strategies: Study 5

Does Early Intervention Improve Weight Loss Outcomes Among Individuals Enrolled in an Internet-based Weight Loss Program?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02163252
Enrollment
110
Registered
2014-06-13
Start date
2014-02-28
Completion date
2014-07-31
Last updated
2015-02-19

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

Conditions

Obesity

Brief summary

The purpose of this study is to examine whether providing additional intervention support to individuals with lower than expected weight loss within the initial stages of an internet-based behavioral weight loss program improves weight loss outcomes at Week 12, compared to the internet program alone.

Interventions

BEHAVIORALStandard
BEHAVIORALEarly Intervention

Sponsors

The Miriam Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* age 18-70 years * BMI \>=25 kg/m2 * No health problems that make weight loss or unsupervised exercise unsafe * English speaking * Access to computer/internet

Exclusion criteria

* report a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire 62 (PAR-Q; items 1-4). * Individuals endorsing joint problems, prescription medication use or other medical conditions that could limit exercise will be required to obtain written consent to participate from a health care provider * are currently pregnant or intend to become pregnant in the next 12 months * are planning to move outside of the state within the next 4 months

Design outcomes

Primary

MeasureTime frame
Change in weight12-week

Secondary

MeasureTime frameDescription
frequency of self-monitoring12 weeksA secondary aim is to examine whether the provision of additional intervention support improves the frequency of self-monitoring as measured by the number of days that an individual logged their calorie information on the study website.
exercise minutes12 weeksA secondary aim is to examine whether the provision of additional intervention support improves the number of exercise minutes reported each week, as logged by the individual on the study website.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026