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Clinical Trials/NCT03801174
NCT03801174CompletedNot Applicable

Using Partners to Enhance Long-Term Weight Loss

University of Wisconsin, Madison1 site in 1 country346 target enrollmentStarted: January 15, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
346
Locations
1
Primary Endpoint
Body Weight (kg)

Study Overview

Brief Summary

This study involves an evaluation of the role of domestic partner support in a comprehensive weight loss initiation and maintenance program.

Detailed Description

Couples will be randomized to a comprehensive weight program directed at patients alone or involving their partners. In months 1-6, all patients will receive group-based weight loss program. In months 7-18, all patients will receive a telephone-based weight loss maintenance intervention. In the partner-assisted arm only, partners will participate in the intervention, learning and practicing communication skills and support strategies. In months 19-24, intervention will be withdrawn to examine sustainability of effects.

Due to COVID-19, option of doing screening and outcome assessment visits and attending the group classes (including exercise) remotely via a video conference may be available. COVID-19 survey will be administered every 3 month starting at screening/enrollment visit.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 74 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •(patients):
  • •Aged 18-74 years
  • •BMI 27-29.9 kg/m2 plus at least one obesity-related comorbidity or BMI >=30 kg/m2
  • •Cohabitating and at least daily contact with a spouse/domestic partner
  • •Access to reliable transportation
  • •Desire to lose weight
  • •Speak and read English
  • •Agree to attend visits per protocol
  • •Score of at least 4 out of 6 on Callahan cognitive screener
  • •Able to stand without assistance for weight measurements without assistance
  • •Possess individual email address
  • •Possess individual smart phone with data and texting plan
  • •Able to complete online screener without assistance
  • •Able to use a smartphone, tablet or computer with a video camera or webcam and microphone to download apps and to connect to a video conference call without assistance

Exclusion Criteria

  • •(patients):
  • •Currently or planning to become pregnant or breastfeeding in the study timeframe
  • •Weight loss ≥ 5 lb in the month prior to screening
  • •Currently enrolled, or enrolled in previous 3 months, in a clinical or research program focusing on lifestyle change that could affect weight
  • •Significant dementia, schizophrenia, psychosis, or drug or alcohol abuse
  • •Chronic or unstable illness that would limit ability to participate (e.g., recent hospitalization; unstable heart disease in the 6 months prior to screening, chronic kidney disease stage 4 or higher)
  • •Living a nursing home or receiving visits from a home health care agency
  • •Planning to relocate in the next 2.5 years
  • •Current use of prescription or over-the-counter weight loss medications
  • •History of bariatric surgery or planning to have bariatric surgery in the study timeframe
  • •Impaired hearing
  • •Currently receiving, or received in the past 6 months, treatment for cancer other than skin cancer
  • •Use of insulin, sulfonylureas, or meglinitides for diabetes
  • •High diuretic dose
  • •Exertional chest pain, dizziness, or lightheadedness
  • •Pain or other condition than prohibits mild-moderate exercise
  • •History of ascites requiring paracentesis
  • •Inclusion criteria (partner):
  • •Aged 18 or older
  • •Willing to participate
  • •Access to reliable transportation
  • •Speak and read English
  • •Score of at least 4 out of 6 on Callahan cognitive screener
  • •Possess smart phone with data and texting plan (not shared with index patient)
  • •Possess email address (not shared with index patient)
  • •Able to complete online screener without assistance
  • •Exclusion criteria (partner):
  • •BMI <18.5 kg/m2
  • •Significant dementia, schizophrenia, psychosis, or drug or alcohol abuse
  • •Residing in a nursing home or receiving home health care
  • •Impaired hearing
  • •Currently receiving, or received in the past 6 months, treatment for cancer other than skin cancer
  • •Chronic or unstable illness that would limit ability to participate (e.g., recent hospitalization; unstable heart disease in the 6 months prior to screening)

Arms & Interventions

Partner-assisted intervention

Experimental

Patients and partners will receive intervention

Intervention: Partner-assisted intervention (Behavioral)

Patient-only intervention

Active Comparator

Patients will receive intervention

Intervention: Patient-only intervention (Behavioral)

Outcomes

Primary Outcomes

Body Weight (kg)

Time Frame: 24 months

Measured on a calibrated, digital scale to the nearest 0.1 kg, assessed every 6 months with 24 months as primary endpoint

Secondary Outcomes

  • Caloric Intake (kcal)(24 months)
  • Physical Activity(24 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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