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A Brief Outpatient Problem-solving Intervention to Promote Healthy Eating and Activity Habits in Adolescents

A Pilot Study of the Healthy Living Study, a Randomized Controlled Trial of a Brief Outpatient Problem-solving Intervention to Promote Healthy Eating and Activity Habits in Adolescents.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01699958
Enrollment
50
Registered
2012-10-04
Start date
2011-06-30
Completion date
2012-02-29
Last updated
2012-10-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Behavior

Keywords

Problem solving therapy, Behavior change

Brief summary

The purpose of this study is to refine, evaluate the feasibility, and to estimate the effect of the healthy Living Study, a brief outpatient problem-solving intervention to promote healthy eating and activity habits in adolescents.

Detailed description

This study will refine, evaluate the feasibility, and estimate the effect of a brief problem-solving intervention to promote healthy eating and activity habits in adolescents. Intervention participants will receive 2 sessions of individual behavioral counseling on problem-solving skills utilizing educational videos, handouts, and worksheets. Intervention participants will be asked to generate unique health goals and practice utilizing problem-solving skills to achieve these goals.Control participants will receive standard of care. Outcomes will explore the ability to shorten the intervention, integrate the intervention into busy outpatient clinics, and estimate the effect of the intervention on confidence to maintain or improve healthy habits and to improve problem-solving skills.

Interventions

Participants will receive 2 individual sessions teaching and reviewing problem-solving skills.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Stanford University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
13 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* 13-18 years old * Able to read and speak English * Patient of the Lucile Packard Children's Hospital teen clinic, weight clinic, or mobile teen van

Exclusion criteria

* History of purging within the prior 12 months

Design outcomes

Primary

MeasureTime frameDescription
Feasibility to conduct a brief problem-solving intervention in a busy academic outpatient setting.From recruitment of the first participant to completion of the intervention by the last participant, anticipated duration of time: 7-8 monthsFeasibility will be measured in the following ways: 1. Refinement of the intervention by the end of the study to a reasonable length to compliment average patient clinic visits with a goal of 30 minutes or less 2. Minimal disruption of clinic flow measured through clinic provider and staff satisfaction surveys and qualitative comments during the course of the intervention

Secondary

MeasureTime frameDescription
Change in problem-solving skillsChange from baseline to 1-2 monthsParticipants will complete survey questions modified from the Social Problem-Solving Inventory for Adolescents (SPSI-A) both pre-intervention and post-intervention. These questions provide an assessment of problem-solving skills and are scored on a Likert scale of 1-5 with 5=more positive/constructive problem-solving skills. Change in overall mean score from pre- to post- intervention will be compared within intervention and control groups and between groups. Duration of time between pre- and post- intervention will average 1-2 months.
Change in confidence to maintain or improve healthy eating habitsChange from baseline to 1-2 monthsParticipants will complete pre- and post- intervention questions on confidence to maintain or improve healthy eating habits. An example question: How confident are you that you could change or maintain your eating patterns to limit soda to \<1 can/day. Questions will be scored on a Likert scale of 1-6 with 6=very confident. Change in overall mean score from pre- to post- intervention will be compared within intervention and control groups and between groups. Duration of time between pre- and post- intervention will average about 1-2 months.
Sufficient recruitment and retention ratesFrom recruitment of the first participant to completion of the intervention by the last participant, anticipated duration of time: 7-8 monthsDetailed records of patients approached, consented, randomized, and completing the study will be maintained. These records will be reviewed at the conclusion of the study to gauge patient interest in participating in a problem-solving intervention in the outpatient setting.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026