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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02206529
Other study ID # 211098
Secondary ID
Status Completed
Phase N/A
First received July 21, 2014
Last updated October 11, 2017
Start date May 2012
Est. completion date May 2014

Study information

Verified date October 2017
Source Kaiser Permanente
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to develop a Social Network Engagement (SNE) Intervention that will be integrated into a standard treatment program for childhood overweight. The investigators will conduct a pilot trial of SNE to assess feasibility and to estimate its effectiveness compared with historical controls who received standard treatment. The historical controls will be participants in the FOCUS trial (Family Overweight: Comparing Use of Strategies; NCT00746629).


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date May 2014
Est. primary completion date May 2013
Accepts healthy volunteers No
Gender All
Age group 7 Years to 13 Years
Eligibility Inclusion Criteria Children

- Age 7-13 years

- At or above the 85th percentile for age- and gender-specific BMI

Parents

• At least one overweight parent (BMI>25.0)

Parents and children

- English-speaking and at least at a second-grade reading level

- Live <50 miles from the treatment site.

Exclusion Children

- Conditions known to promote obesity (e.g., Prader-Willi),

- Participation in another weight control program

- Recently started taking weight-affecting medications (e.g., stimulants).

Parents and children

- Disability or illness that would preclude them from engaging in at least moderate-intensity physical activity,

- Current or prior diagnosed eating disturbance

- Thought disorder, suicidality, or substance abuse disorder

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Social Network Engagement+Std Treatment

Standard Treatment
Standard Treatment = family-based behavioral pediatric obesity treatment, as per protocol outlined in FOCUS trial (Family Overweight: Comparing Use of Strategies; NCT00746629)

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Kaiser Permanente

Outcome

Type Measure Description Time frame Safety issue
Other SSQ (Social Support Questionnaire-Short Form) Global social support measure, assessed as possible mediator of effect of intervention on primary and secondary outcomes. 20 weeks after baseline
Other QRI (Quality of the Relationship Index) Relationship-specific social support measure, assessed as possible mediator of effect of intervention on primary and secondary outcomes. 20 weeks after baseline
Other SPSI-R (Social Problem-Solving Index-for Research) Measure of parental skill in problem-solving, assessed as possible mediator of effect of intervention on primary and secondary outcomes. 20 weeks after baseline
Other Behavioral Skill Assessment Process measure of parental use of skills taught during intervention 20 weeks after baseline
Other WMSI (Weight Management Support Index) Measure of parental perceived social support related to weight management, assessed as possible mediator of primary and secondary outcomes. 20 weeks after baseline
Primary Child BMI Z-score 20 weeks after baseline
Primary Child BMI Z-score One year post-treatment
Secondary Peds QL (child self-report and parent report) Pediatric Quality of Life Score 20 weeks after baseline
Secondary Parent BMI Intervention is aimed at the parent-child dyad, so parent weight status is assessed. 20 weeks after baseline
Secondary Peds QL (child self-report and parent report) Pediatric Quality of Life Score One year post-treatment
Secondary Parent BMI Intervention is aimed at the parent-child dyad, so parent weight status is assessed. One year post-treatment
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