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Internet Treatment for Weight Loss in Primary Care

Not Applicable
Completed
Conditions
Overweight
Obese
Interventions
Behavioral: Motivational Interviewing
Behavioral: Treatment as usual with primary care physician
Behavioral: Nutritional Counseling
Registration Number
NCT01558297
Lead Sponsor
Yale University
Brief Summary

This study will test the effectiveness of two distinct treatments for weight loss:

1. Motivational Interviewing

2. Nutritional Counseling. These treatments will be compared to Treatment as Usual. Participants will be recruited through local primary care offices.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
89
Inclusion Criteria
  • BMI 25-55
  • Daily access to internet and phone
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Exclusion Criteria
  • Co-existing physical and/or psychiatric conditions that require more significant treatment (e.g., bipolar disorder, psychotic illnesses), and/or require more intensive treatment or hospitalization (e.g., suicidality, severe mood disorders)
  • Meets criteria for current substance abuse or dependence
  • Currently receiving psychiatric, psychological, behavioral, or pharmacologic treatment that is known to affect weight or eating
  • Pregnant, breastfeeding, or plans to become pregnant during the treatment period
  • Cardiac disease, including ischemic heart disease, congestive heart failure, conduction abnormalities, or a history of heart attack
  • Serious neurologic illnesses (e.g., seizure history) or medical illnesses (e.g., impaired hepatic or renal function)
  • Uncontrolled diabetes, thyroid conditions, or hypertension
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Motivational InterviewingMotivational Interviewing-
Treatment as usualTreatment as usual with primary care physician-
Nutritional CounselingNutritional Counseling-
Primary Outcome Measures
NameTimeMethod
Body Weight in Pounds.6 months after treatment start (Baseline)

Body weight lost in pounds measured 6 months after first treatment session (3 month follow-up after active treatment ends).

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Yale School of Medicine

🇺🇸

New Haven, Connecticut, United States

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