- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02741037
Unidas Por la Vida: A Healthy Lifestyle Intervention for High-risk Latina Dyads
August 16, 2023 updated by: Dara Sorkin, University of California, Irvine
Mexican American women have significantly elevated rates of obesity and type 2 diabetes.
The proposed study tests a novel intervention that capitalizes on an existing important family dyad (mothers and their adult daughters) to foster clinically significant and long-lasting health behavior change.
If found to effective, this intervention strategy has great potential to address health disparities in this, and other, at-risk populations.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Approximately half of Mexican-American women report having a sedentary lifestyle, and nearly 78% are overweight or obese.
Compared to women in all other ethnic groups, Mexican-American women have the highest lifetime risk of type 2 diabetes.
The development of culturally appropriate lifestyle interventions for this population is an urgent priority, and the proposed study accordingly will investigate a novel dyadic intervention designed to improve health behaviors and promote weight loss in two at-risk members of the same family: mothers with type 2 diabetes and their overweight/obese adult daughters who are at risk for developing diabetes.
The intervention, Unidas por la Vida (United for Life), capitalizes on the importance of the family in Latino culture to mobilize an existing family dyad as a source of mutual support that is likely to foster greater and longer-lasting health behavior change.
The study builds on a successful pilot study (R34 DK083500) that established the feasibility and acceptability of this dyadic behavioral lifestyle intervention in a high-risk sample of Mexican-American family members who share a risk for diabetes and its complications.
The 16-week intervention was modeled after the Diabetes Prevention Program (DPP), but was adapted for use with mother daughter pairs and to be community-based and, thus, more easily accessible to low-income Latinas.
Preliminary data from the Unidas pilot study indicated that the dyadic intervention promoted significant weight loss.
The proposed study extends the successful pilot study to: 1) target weight loss > 5% of baseline body weight and to foster maintenance using a tapered intervention, 2) add comparison groups that permit evaluation of the improvement uniquely associated with the partner intervention, and 3) assess theoretically derived mediators of the intervention.
Participants (N=460 mother-adult daughter dyads) will be randomized into one of three conditions: 1) dyadic (mother-daughter) participation in a Unidas partner intervention (Arm 1); 2) individual participation (mothers alone; unrelated daughters alone) in a Unidas individual intervention (Arm 2); and 3) mother-daughter dyad in a usual care only condition (Arm 3).
Study Type
Interventional
Enrollment (Actual)
710
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
Mothers:
- Are Mexican-American
- Are age 18 and older
- Have a body mass index (BMI) between 25 kg/m2 and 43 kg/m2.
- Are diagnosed with type 2 diabetes
- Live within a 25 mile radius of your adult daughter
- Are fluent in either Spanish or English as your primary language
- Are able to understand and sign an informed consent
Adult daughters:
- Are Mexican-American
- Are age 18 and older
- Have a body mass index (BMI) between 25 kg/m2 and 43 kg/m2.
- Live within a 25 mile radius of your mother
- Are fluent in either Spanish or English as your primary language
- Are able to understand and sign an informed consent
Exclusion Criteria:
- Are male
- Have a visual or hearing impairment, documented psychiatric and/or life-threatening illness that precludes the ability to participate in a weight loss program and/or provide consent.
- Are a mother with diabetes who is not able to start an exercise regimen or are likely to be injured (e.g., have uncontrolled high blood pressure).
- Are pregnant or become pregnant during the course of the study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Dyadic lifestyle intervention
Mothers and daughters participate in the Unidas partner intervention together.
|
Dyadic lifestyle intervention: The dyadic behavioral lifestyle intervention was modeled after the Diabetes Prevention Program (DPP), and was adapted to make it more easily accessible to low-income Latinas.
In addition, this intervention arm has a dyadic component to examine the effectiveness of mothers and daughters engaging in the lifestyle intervention together as partners.
Participants also will receive usual care.
Usual Care: Mother and daughter participants will receive Usual Care.
|
|
Experimental: Individual lifestyle intervention
Mothers participate in the Unidas intervention alone, without their related daughters.
Unrelated daughters participate in the Unidas intervention alone without their related mothers.
|
Usual Care: Mother and daughter participants will receive Usual Care.
Individual lifestyle intervention: The individual behavioral lifestyle intervention was modeled after the Diabetes Prevention Program, and was adapted to make it more easily accessible to low-income Latinas.
Mothers participate in the Unidas intervention alone, without their related daughters.
Unrelated daughters participate in the Unidas intervention alone without their related mothers.
Participants also will receive usual care.
|
|
Other: Usual Care
Mothers and daughters receive usual care.
|
Usual Care: Mother and daughter participants will receive Usual Care.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Longitudinal % change in body weight
Time Frame: 6, 12, and 18 months
|
The study will compare longitudinal % change in body weight across the three study arms.
|
6, 12, and 18 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Longitudinal change in dietary intake
Time Frame: 6, 12, and 18 months
|
The study will examine whether changes in dietary intake are greatest among women in the partner intervention, compared to women in an individual intervention or in usual care, and to examine whether changes in dietary intake mediate the effects of the intervention on weight status and maintenance.
Dietary intake will be measured with the Spanish version of the 2005 Block Food Frequency Questionnaire (FFQ).
This instrument assesses portion sizes and frequency of consumption of over 100 food items, including foods selected for their cultural appropriateness for Mexican Americans to provide validated estimates of energy intake (total kilocalories) and macronutrient intake (including fat, carbohydrates and dietary fiber).
|
6, 12, and 18 months
|
|
Longitudinal change in physical activity
Time Frame: 6, 12, and 18 months
|
The study will examine whether changes in physical activity are greatest among women in the partner intervention, compared to women in an individual intervention or in usual care, and to examine whether changes in physical activity mediate the effects of the intervention on weight status and maintenance.
The 7-day physical activity recall (PAR) will be used to assess physical activity at each study time point.
Participants will be asked to estimate the number of hours spent each day (starting with the current day and working backwards) in sleep and in moderate, hard, and very hard physical activities.
|
6, 12, and 18 months
|
|
Longitudinal change in interpersonal processes
Time Frame: 6, 12, and 18 months
|
The study will examine whether changes in theoretically-derived mediating mechanisms, such as interpersonal processes, are greatest among women in the partner intervention, compared to women in the individual intervention or in usual care to examine whether changes in these processes mediate the effects of the intervention on dietary intake and in physical activity.
Well-established methods of social network and social exchange assessment will be used to obtain detailed information about the involvement of participants' social network members in health-related social support, social control, and/or social undermining.
Participants will be asked to identify social network members who have helped them make healthy lifestyle changes (social support), have prompted or urged them to do more to make such changes (social control), and/or have interfered (intentionally or unintentionally) with their efforts to make such changes (social undermining).
|
6, 12, and 18 months
|
|
Longitudinal change in mother-daughter processes of mutual influence
Time Frame: 6, 12, and 18 months
|
The study will examine actor-partner interdependence models to explore group differences in mother-daughter processes of mutual influence across the study arms, with this mutual influence expected to be greater and more strongly related to the primary and secondary outcomes for women in the partner intervention, compared to women in the individual intervention or in usual care.
|
6, 12, and 18 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Dara H Sorkin, Ph.D., University of California, Irvine
- Principal Investigator: Karen S Rook, Ph.D., University of California, Irvine
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2016
Primary Completion (Actual)
July 1, 2021
Study Completion (Actual)
July 1, 2021
Study Registration Dates
First Submitted
March 31, 2016
First Submitted That Met QC Criteria
April 12, 2016
First Posted (Estimated)
April 18, 2016
Study Record Updates
Last Update Posted (Actual)
August 21, 2023
Last Update Submitted That Met QC Criteria
August 16, 2023
Last Verified
August 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20097225
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Obesity
-
Dr. Christopher McGowanRecruitingObesity Prevention | Obesity Recidivism | Obesity and Overweight | Obesity and Obesity-related Medical ConditionsUnited States
-
Central Hospital, Nancy, FranceNot yet recruiting
-
Helsinki University Central HospitalKarolinska Institutet; Folkhälsan Researech CenterEnrolling by invitation
-
Istanbul Medipol University HospitalMedipol UniversityCompletedObesity, Morbid | Obesity, Adolescent | Obesity, Abdominal | Weight, Body | Obesity, VisceralTurkey
-
Dr. Christopher McGowanRecruitingObesity Prevention | Obesity Recidivism | Obesity and Overweight | GLP-1 | Obesity and Obesity-related Medical Conditions | Ablation TechniquesUnited States
-
Azienda Ospedaliero-Universitaria Consorziale Policlinico...Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies; Istituti... and other collaboratorsCompletedMorbid Obesity | Metabolically Healthy ObesityItaly
-
Queen Fabiola Children's University HospitalNot yet recruitingMorbid Obesity | Adolescent Obesity | Bariatric SurgeryBelgium
-
Washington University School of MedicinePatient-Centered Outcomes Research Institute; Pennington Biomedical Research... and other collaboratorsCompletedOvernutrition | Nutrition Disorders | Overweight | Body Weight | Pediatric Obesity | Body Weight Changes | Childhood Obesity | Weight Gain | Adolescent Obesity | Obesity, Childhood | Overweight and Obesity | Overweight or Obesity | Overweight AdolescentsUnited States
-
University of ÉvoraNot yet recruitingObesity and Obesity-related Medical Conditions
-
The Hospital for Sick ChildrenCompleted
Clinical Trials on Dyadic lifestyle intervention
-
Concordia University, MontrealCentre de Recherche de l'Institut Universitaire de Geriatrie de MontrealActive, not recruiting
-
National Cheng Kung UniversityNational Health Research Institutes, TaiwanCompleted
-
VA Office of Research and DevelopmentCompleted
-
National Cheng Kung UniversityNational Health Research Institutes, TaiwanCompletedChronic Kidney DiseasesTaiwan
-
University of PittsburghCompleted
-
The University of Hong KongCompleted
-
Vanderbilt UniversityVanderbilt University Medical CenterCompletedNurse-Patient Relations | Pediatric Cancer | Narrative Medicine | Growth, PosttraumaticUnited States
-
National Taipei University of Nursing and Health...Chang Gung Memorial HospitalRecruitingProstate Cancer (Adenocarcinoma)Taiwan
-
Jiangsu Taizhou People's HospitalRecruitingEnd Stage Renal Disease on DialysisChina
-
Sun Yat-sen UniversityCompleted