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Remote Weight Management Program for Obese Women

Cedars-Sinai Medical Center logo

Cedars-Sinai Medical Center

Status

Completed

Conditions

Weight Loss

Treatments

Behavioral: Motivational Interviewing counseling on the Mediterranean diet and weight checks at regular intervals

Study type

Interventional

Funder types

Other

Identifiers

NCT05635097
00002292

Details and patient eligibility

About

The purpose of the research project is to see if counseling on the Mediterranean diet combined with motivational interviewing via a telemedicine platform (Zoom) while using smart technology ("smart" scales and tape) improves participants' weight loss, reduces waist circumference, and improves satisfaction with their care.

Full description

The investigators will evaluate a formal remote weight management and follow-up program, utilizing a technology-based intervention using the Renpho application paired with a smart scale and smart tape measure. The primary communication technologies will be the REDCap and Zoom platforms.

Renpho's smart body fat scale and tape measure are health applications that sync with fitness applications such as Apple Health, MyFitnessPal, Fitbit, and Samsung Health. The Renpho Bluetooth-enabled smart scale and smart tape devices will allow participants to sync with the Renpho application on their smartphone to automatically upload data such as weight, BMI, and WC to their phone. The project leader will review participants' self-reported weights and WC fortnightly. The participants will be asked to complete a post-participation satisfaction survey that includes a 5-point scale ("strongly agree", "agree", "neutral", "disagree:", to "strongly disagree") Likert-style questions.

Expected Outcomes. The primary outcomes for this eight-week intervention are to achieve a clinically significant reduction in weight of at least 5-10 % and at least 2.5 inches reduction in WC per participant from baseline.

Enrollment

30 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Women with a clinical diagnosis of obesity (BMI ≥30 kg/m2),
  2. Age of 18 years or older,
  3. English-speaking participants with access to a smartphone device
  4. At least one cardiovascular risk factor (at least one clinical diagnosis of the following conditions: hypertension, dyslipidemia, type 2 diabetes, pre-diabetes, sleep apnea, family history of heart disease, cigarette smoking, inactivity, preeclampsia, gestational diabetes, gestational hypertension, preterm birth, rheumatological diseases, or premature menopause).

Exclusion criteria

  1. Must not be taking medications specifically for weight loss or currently participating in a weight loss program,
  2. Must not be pregnant or breast-feeding,
  3. Women without a clinical diagnosis of obesity (BMI < 30 kg/m2)
  4. Must not have lost >3 kg body weight or dramatically changed physical activity patterns within the past six months,
  5. Clinical diagnosis of eating disorders
  6. Clinical diagnosis of uncontrolled hypertension or neurological or psychological disorders
  7. Must not have any obesity-related surgery within the past six months (i.e., gastric bypass).

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

One group intervention
Other group
Description:
One group without comparator
Treatment:
Behavioral: Motivational Interviewing counseling on the Mediterranean diet and weight checks at regular intervals

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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