Physical Inactivity Clinical Trial
Official title:
Active Moms: A Feasibility Study of a Community-Based and Home-Based Physical Activity Intervention for Low-Income, Ethnic-Minority Mothers
NCT number | NCT05540509 |
Other study ID # | PHS 11-252 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | May 23, 2012 |
Est. completion date | May 1, 2013 |
Verified date | September 2022 |
Source | California State University, Long Beach |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Despite the health benefits of physical activity, increasing regular physical activity levels among low-income, ethnic-minority mothers has remained a significant challenge. The current mixed-methods feasibility study explored the impact that a three-month community-based (CBI) and a home-based intervention (HBI) had on improving physical activity and fitness levels, as well as psychosocial outcomes (self-efficacy and social support) among low-income, ethnic-minority mothers. These results support the efficacy of CBIs and HBIs in improving PA and fitness levels and have important implications for improving health outcomes among low-income, ethnic-minority mothers.
Status | Completed |
Enrollment | 30 |
Est. completion date | May 1, 2013 |
Est. primary completion date | May 1, 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 18 years of age or older - a mother of a young child (<10 years of age) - fluent in either Spanish or English - Sedentary (i.e., not engaging in 90 minutes or more of moderate or vigorous physical activity per week) Exclusion Criteria: - Not medically cleared by a doctor or by a medical history screener to engage in moderate-intensity physical activity - Currently pregnant |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
California State University, Long Beach |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Physical Activity from baseline to 3 months post-intervention | Self-reported duration of moderate/vigorous physical activity was assessed using the Check and Line Questionnaire (CALQ), with higher numbers representing greater average minutes of moderate/vigorous-intensity PA completed/day over a three-day assessment period. Objective physical activity was assessed using the Fitbit One (2009 version), which is an accelerometer worn on the hip (clipped to a participant's clothing at the waist). For the current study, very active minutes were examined (measure of basal metabolic rate/minute). Activity data was averaged across the three days that the Fitbit was worn, with greater number of very active minutes indicating greater daily moderate/vigorous-intensity physical activity levels. | Self-reported and fitbit physical activity assessments were conducted at baseline and at one, two, and three months post-intervention. | |
Primary | Change in Cardiorespiratory Fitness from baseline to 3 months post-intervention | Cardiorespiratory fitness was assessed via predicted relative maximum oxygen consumption, also known as relative VO2 max (ml/kg/min) after participants completed a timed mile walk, with a greater relative VO2 max being an indicator of greater cardiorespiratory fitness. | Cardiorespiratory fitness assessments were conducted at baseline and at one, two, and three months post-intervention. | |
Primary | Change in Muscle Endurance from baseline to 3 months post-intervention | Muscle endurance was assessed by the number of modified push-ups completed in correct form, with a greater number of 90° push-ups completed representing greater muscular endurance. | Muscle endurance assessments were conducted at baseline and at one, two, and three months post-intervention. | |
Primary | Change in Flexibility from baseline to 3 months post-intervention | Flexibility was assessed by a modified sit and reach test (in inches) where mothers were instructed to reach forward as far as they could with their hands over each other, over a three-foot ruler, without removing their body from the wall and holding this position for at least two seconds, with greater inches indicating greater flexibility. | Flexibility assessments were conducted at baseline and at one, two, and three months post-intervention. | |
Secondary | Change in Physical Activity Self-Efficacy from baseline to 3 months post-intervention | Physical Activity Self-efficacy was assessed using the Barriers Self-Efficacy Scale. The 14-item Barriers Self-Efficacy Scale measures a mother's level of confidence in engaging in physical activity despite barriers experienced over the next three months, with higher scores (range=0-100) reflecting higher self-efficacy for physical activity in the face of barriers. | Physical Activity Self-efficacy assessments were conducted at baseline and at one, two, and three months post-intervention. | |
Secondary | Change in Fitness Self-Efficacy from baseline to 3 months post-intervention | Fitness Self-efficacy was assessed using the Self-Efficacy for Physical Performance Scale. The 5-item Self-Efficacy for Physical Performance Scale measures a participant's self-efficacy to currently perform multiple activities that improve fitness (e.g., walking a mile, doing push-ups), with higher scores (range=0-100) indicating higher self-efficacy for fitness. | Fitness Self-efficacy assessments were conducted at baseline and at one, two, and three months post-intervention. | |
Secondary | Change in Social Support from baseline to 3 months post-intervention | Social support for physical activity was assessed using the 15-item Social Support for Exercise Survey. The Social Support for Exercise Survey measures the degree of social support received from one's family and friends to engage in physical activity, with higher scores (range=0-75) reflecting more social support received from each of these support networks. | Social support assessments were conducted at baseline and at one, two, and three months post-intervention. |
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