The Wildcat Wellness Coaching Trial

NCT01845480 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2017-02-24

No results posted yet for this study

Summary

Female children (aged 8-13 years) will be recruited through posted flyers, newspaper ads, and word of mouth in the Manhattan, KS area. After laboratory assessment, recruited participants will be randomly assigned to either healthful eating and physical activity skills coaching or general health education coaching intervention conditions. For both conditions, research assistants will serve as wellness coaches and deliver 12 intervention sessions in the home of each participating child.

Assessments will be completed at baseline, intervention end (3 months), and follow-up (6 months), comprising biomedical and psychosocial measures. Biomedical measurements to be obtained include:

* body composition (DEXA, tetrapolar bioimpedance, body mass index, waist circumference)
* blood pressure (automated sphygmomanometer),
* pulmonary function tests (forced expiratory flow in 1-sec, forced vital capacity, forced expiratory flow at 25-75% of vital capacity),
* unstimulated whole (mixed) saliva passive drool to detect markers of inflammation,
* and physical activity levels (7-day accelerometry).

Psychosocial measurements include:

* fruit and vegetable consumption (Child Dietary Questionnaire)
* self efficacy,
* enjoyment
* quality of life (Peds QL).

Inclusion criteria are:

* being female
* aged 8-13 years
* with parental consent,
* residing within a 40-minute drive
* being available for 12 home coaching visits and three lab assessments.

Exclusion criteria are

* having developmental delay or psychiatric problems,
* any illness, injury, condition, or disease that would prevent participation in moderate-to-vigorous physical activity,
* taking weight-altering medications
* participating in any other health behavior change program.

The objectives of this study are to determine

* whether both types of the home-based coaching interventions are feasible
* whether the healthful eating and physical activity skills coaching intervention is more efficacious, relative to the general health education coaching group, in preventing increases in body fat percentage, body mass index percentile, waist circumference, systolic and diastolic blood pressure, and sedentary behavior
* whether the healthful eating and physical activity skills coaching intervention is more efficacious, relative to the general health education coaching group, in facilitating increases in quality of life, moderate-to-vigorous physical activity, enjoyment of physical activity and fruit and vegetable consumption, and self-efficacy for physical activity and fruit and vegetable consumption.

We hypothesize that the research project will be successful in recruiting and retaining participating families, training research assistants to deliver the intervention components, and that both of the coaching conditions will be well received and appreciated by participating families. We hypothesize that the healthful eating and physical activity skills coaching intervention will be more effective than the support coaching condition in preventing increases in blood pressure, airway dysfunction and adiposity. We expect that both intervention conditions will show improvements to pediatric quality of life measures, but that the healthful eating and physical activity skills coaching intervention will be more effective than general health education coaching condition in increasing physical activity, physical activity enjoyment and self efficacy, fruit and vegetable consumption, and fruit and vegetable enjoyment and self-efficacy.

Conditions

  • Health Promotion and Obesity Prevention

Interventions

BEHAVIORAL

Wellness coaching

Wellness coaching that includes modeling, goal setting, self-monitoring, social support, and health behavior education

Sponsors & Collaborators

  • Kansas State University

    lead OTHER

Principal Investigators

  • Richard R. Rosenkranz, Rosenkranz · Kansas State University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
8 Years
Max Age
13 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-08-20
Primary Completion
2017-09-20
Completion
2017-10-13

Countries

  • United States

Study Locations

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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 NCT01845480 on ClinicalTrials.gov