CHOICE to AVOID or RESIST

Part of paid clinical trials in Beverly Hills, California.

Sponsor
Cedars-Sinai Medical Center
Study ID
NCT06521021
Status
Recruiting
Apply to this trial

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 80 Years
Healthy Volunteers
Accepted

Interventions

  • AVOID — BEHAVIORAL
    Behavioral: Home food environment and grocery delivery (AVOID) Participants will receive coaching (Zoom and/or email/text) to modify their home food environment and alter cues to promote healthy food choices Behavioral: WW Participants assigned to all arms will receive of coaching (Zoom and/or email/text) and commercially-available weight management program focusing on diet, physical activity and mindset skills.
  • RESIST — BEHAVIORAL
    Behavioral: Inhibitory control training (RESIST) Participants assigned to RESIST will receive coaching (Zoom and/or email/text) and gamified inhibitory control training. Behavioral: WW Participants assigned to all arms will receive coaching (Zoom and/or email/text) and commercially-available weight management program focusing on diet, physical activity and mindset skills.

Study Details

This trials will formally test whether participants' active choice of self-regulatory strategies (AVOID or RESIST) leads to greater adherence to weight management strategies by comparing the CHOICE arms to the randomized arms of the parent intervention, AVOID/RESIST (IRB STUDY00001652: AVOID-RESIST).

Key Dates

First listed
Jul 25, 2024
Start date
Jun 1, 2026
Status verified
Feb 2026
Primary completion
Jul 1, 2027
Completion
Jul 1, 2027

Study Design

Enrollment
60 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Other: WW + Home modification and grocery delivery (AVOID)
    WW + modification of home food environment + online grocery shopping and delivery Arm assignment is selected by participant.
  • Other: WW + Inhibitory control training (RESIST)
    WW + daily gamified inhibitory control training Arm assignment is selected by participant.

Primary Outcome Measure

Completion Rate of Follow-up Visits [ Time Frame: 3 Month, 6 Month ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Cedars-Sinai Medical CenterBeverly HillsCalifornia90211
Julissa Ruiz, BS
[email protected]
Sarah-Jeanne Salvy, PhD
[email protected]
Sarah-Jeanne Salvy, PhD (PRINCIPAL_INVESTIGATOR)

Find similar trials in Beverly Hills, CA

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By condition
Obesity / overweight
By specialty
EndocrinologyMetabolic healthWeight loss
By research site
Cedars-Sinai Medical Center· Beverly Hills, CA

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