Web-based Physical Activity Intervention for Latinas

Inactivity Clinical Trial

Official title:

Promoting Physical Activity in Latinas Via Interactive Web-based Technology

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03491592
• Other study ID #: R01CA159954
• Secondary ID: R01CA159954
• Status: Completed
• Phase: N/A
• Start date: June 1, 2018
• Est. completion date: April 1, 2022

Study information

• Verified date: February 2023
• Source: Brown University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This renewal builds upon our successful culturally adapted PA intervention for Latinas (Pasos Hacia La Salud, R01CA159954) and expands its focus to the critical area of maintenance of behavior change. This study will test an enhanced version of the original internet intervention in order to achieve greater increases in PA and longer term maintenance. Investigators propose to test this newly developed enhanced intervention (Enhanced Intervention) compared to the original Pasos Hacia La Salud Intervention (Original Intervention) in a 24-month randomized trial (N=300).

Description:

In the U.S., Latina women report higher rates of inactivity than their non-Hispanic White and male counterparts, and are disproportionately affected by related health conditions (e.g., cancer, hypertension, heart disease, stroke, diabetes). To address this public health crisis, evidence-based interventions that utilize state-of-the-art technology, theory and methods are needed to increase physical activity (PA) among this high-risk population. Recently, our team conducted a randomized controlled trial (N=205) to test the efficacy of a 6-month culturally adapted, individually tailored, Spanish-language Internet-based PA intervention among Latinas (Pasos Hacia La Salud, R01CA159954) vs. a Wellness Contact Control Internet Group. Increases in minutes/week of moderate-to-vigorous physical activity (MVPA) were significantly greater in the Intervention Group compared to the Control Group at 6 and 12 months (p < .01) but still did not reach levels recommended in the national physical activity guidelines. As improvements in PA in the Intervention Group were significantly associated with website use and increases in self-efficacy, enjoyment, and social support in the parent study, we used these data to inform technology and theory-supported enhancements to the intervention (i.e., text messaging and adaptive goal setting to increase website use and further targeting of the previously mentioned key psychosocial constructs) to achieve even greater increases in PA, and maintain these gains over the long term (24 months) in the renewal of R01CA159954. For the proposed study, 300 Latina women will be randomized to either 1) the original Pasos Hacia La Salud tailored Internet-based PA intervention (Original Intervention) or 2) the data driven, enhanced version of the Pasos Hacia La Salud PA intervention (Enhanced Intervention). We hypothesize that participants in the Enhanced Intervention arm will report significantly more minutes/week of MVPA than participants in the Original Intervention arm at 6 months. We will also examine the maintenance of treatment effects at 12, 18, and 24 months, as well as the costs of delivering the Enhanced vs. Original Intervention programs, and the potential mediators of the intervention-PA relationship. The proposed high reach, low-cost intervention holds great promise in promoting and maintaining the positive health benefits of PA in the lives of Latina women in the United States.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 210
• Est. completion date: April 1, 2022
• Est. primary completion date: April 1, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Female

• Generally healthy (If asthma and/or high blood pressure, may be able to participate with physician consent)

• Sedentary (Less than 60 minutes per week of moderate or vigorous physical activity)

• Self-identify as Hispanic or Latino (or of a group defined as Hispanic/Latino by the Census Bureau

• Must be able to read and write Spanish fluently

• 18 - 65 years of age

• Daily access to a text-message compatible cell phone and to an Internet-connected device through home, work, or their community

Exclusion Criteria:

• History of coronary heart disease (history of myocardial infarction or symptoms of angina),

• Diabetes that requires insulin and does not have a doctor's approval

• Chronic infectious disease- HIV, Hepatitis C but does not have doctor approval

• Orthopedic conditions which limit mobility, any other serious medical condition that would make PA unsafe (based on modified Physical Activity Readiness Questionnaire)

• Hospitalization due to a psychiatric disorder in the past 3 years

• BMI above 45 kg/m2

• Current or planned pregnancy in the next two year

• Moving from area within two years

• Does not have a cellphone capable of sending and receiving text messages

• Not able to receive materials in the mail, either at your own home or at a mailbox

Related Conditions & MeSH terms

• Inactivity

Intervention

Behavioral:
• Enhanced Physical Activity Intervention
Participants in the Enhanced Intervention arm will receive all the intervention components of the Original Intervention described above plus: 1) text messages and adaptive goal-setting to drive participants back to the website and keep them there longer, and 2) data-driven, technology supported enhanced intervention content targeting theoretical constructs that influenced PA behavior in Latinas from the parent study.
• Original Physical Activity Intervention
Participants in the Original Physical Activity intervention arm of the study will receive the original Spanish language, motivationally-tailored, Internet-based physical activity intervention that specifically addresses the Physical Activity barriers and intervention needs/preferences of Latinas.

Locations

Country	Name	City	State
United States	121 South Main Street, Brown University	Providence	Rhode Island

Sponsors (3)

Lead Sponsor	Collaborator
Brown University	National Cancer Institute (NCI), National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in total weekly minutes of physical activity as measured by an accelerometer	For the week prior to each assessment, participants will wear an Actigraph GT3X+ accelerometer which collects min/week of objectively measured MVPA.	Baseline, 6 months, 12, 18 and 24 months