Free Time For Wellness Pilot Effectiveness Trial

NCT06474715 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 89

Last updated 2026-04-24

Study results available
· View outcomes & findings →

Summary

Physical inactivity is pervasive and prevalent in the United States, particularly among women of low socioeconomic position, and women with children. Structural and social barriers make active leisure time a rare commodity creating a pressing health issue because physical inactivity increases the risk of chronic diseases and poor health. The broad objective of this study is to pilot test the Free Time for Wellness (FT4W), an innovative multilevel physical activity intervention to increase physical activity among low-resourced mothers.

Conditions

  • Physical Inactivity

Interventions

BEHAVIORAL

Arms

The intervention includes a task-based interaction (volunteer activities) where cognitive demand is low and interactional roles are clear. The focus is on the task, rather than developing relationships, reducing the pressure of interaction. As the volunteer activities continue, they also offer the opportunity for group members to enhance empathy, another salient component of cross-group relational development. Mediated interaction supports new relational development through a disinhibiting effect, lowering inhibitions and increasing comfort and disclosure

Sponsors & Collaborators

  • Monash University

    collaborator OTHER
  • Loughborough University

    collaborator OTHER
  • University of Iowa

    collaborator OTHER
  • Public Health Institute

    collaborator UNKNOWN
  • Jovie USA, LLC

    collaborator INDUSTRY
  • West Side Campaign Against Hunger

    collaborator UNKNOWN
  • New York City Parks and Recreation

    collaborator UNKNOWN
  • National Institute on Minority Health and Health Disparities (NIMHD)

    collaborator NIH
  • Columbia University

    lead OTHER

Principal Investigators

  • Lauren C Houghton, PhD, MSc · Dept of Epidemiology, MSPH

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-05-30
Primary Completion
2024-10-14
Completion
2025-04-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06474715 on ClinicalTrials.gov