Skip to content

Telephone Delivered Weight Loss, Nutrition, Exercise WeLNES Study

Telephone Delivered Weight Loss, Nutrition, Exercise Study (WeLNES)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04447313
Enrollment
418
Registered
2020-06-25
Start date
2021-03-05
Completion date
2026-11-09
Last updated
2025-11-24

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

Conditions

Obesity-Related Malignant Neoplasm

Brief summary

This phase III trial compares telephone delivered Acceptance and Commitment Therapy to standard behavioral therapy for improving weight loss in overweight or obese participants. Acceptance and Commitment Therapy focuses on increasing willingness to experience physical cravings, emotions, and thoughts while making values-guided committed behavior changes. Acceptance and Commitment Therapy may work better at improving weight loss compared to standard behavioral therapy.

Detailed description

OUTLINE: Participants are randomized to 1 of 2 arms. ARM I: Participants receive ACT telephone coaching over the course of 12 months, calls 1-16 weekly, calls 17-23 biweekly, and calls 24-25 monthly. Call 1 is 30 minutes in duration, while calls 2-25 are each 15-20 minutes in duration. ARM II: Participants receive SBT telephone coaching over the course of 12 months, calls 1-16 weekly, calls 17-23 biweekly, and calls 24-25 monthly. Call 1 is 30 minutes in duration, while calls 2-25 are each 15-20 minutes in duration. Participants are followed up at 6, 12, and 24 months after randomization.

Interventions

OTHERSurvey Administration

Ancillary studies

BEHAVIORALTelephone-Based Intervention

Receive ACT telephone coaching

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
Fred Hutchinson Cancer Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Overweight or obese (body mass index \[BMI\] \>= 27) but not heavier than BMI of 45.5 (measured by weight & height) * Wants to lose weight in the next 30 days * Interested in learning skills to lose weight * Willing to be randomly assigned to either condition * Resides in United States (US) * Has daily access to their own phone and email * Does not have a medical or psychiatric condition that would limit their ability to comply with the behavioral recommendations of the program or pose a risk to the participant during weight loss, including meeting criteria for binge eating disorder, and meeting criteria for severe depression (CESD \>= 25), or a diagnosis of serious heart disease, diabetes, uncontrolled hypertension, or cancer without written confirmation of approval from their physician office * Not pregnant, planning to become pregnant or breastfeeding in the next 12 months * In the past 3 months changed the dosage of prescription medications that can cause a significant change in weight or appetite * Have not lost more than 5% of their weight in the past 6 months * Willing and able to read in English * Not participating in or planning to participate in other weight loss programs * Has not participated in our other ACT intervention studies * Does not meet criteria for combined heavy plus binge drinking * Has access to a Bluetooth-enabled device and Wi-Fi and/or data plan * Is not planning to have or has not recently had (past 12 months) bariatric surgery * For outcome data retention, eligibility criteria included: Willing to complete follow-up surveys, and provide email, phone, and mailing address

Exclusion criteria

* The reverse of the inclusion criteria

Design outcomes

Primary

MeasureTime frameDescription
10% or more weight lossAt 12 months after randomizationWill be measured remotely by cellular-enabled scales. Will compare the two telephone interventions, using logistic regression.

Secondary

MeasureTime frameDescription
Percent weight changeAt 6, 12, and 24-months post randomizationWill be measured remotely by cellular-enabled scales.
Dietary intakeAt 6, 12, and 24-months post randomizationWill be measured with the Fitbit smartphone app food logging feature.
Physical activityAt 6, 12, and 24-months post randomizationWill be measured with the Fitbit Inspire mailed to participants.
Trajectories of weight changeAt 6, 12, and 24-months post randomizationWill compare between the two arms, with time as the independent variable using mixed effects modeling with linear, quadratic, and cubic effects of time.

Countries

United States

Outcome results

None listed

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