A Pilot Efficacy and Implementation Study of the Strengths Intervention Project



Status:Recruiting
Conditions:Psychiatric
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:13 - 15
Updated:4/6/2019
Start Date:May 4, 2018
End Date:June 2019
Contact:Elizabeth A Friedrich, BA
Email:friedriche@email.chop.edu
Phone:2674251345

Use our guide to learn which trials are right for you!

The purpose of this study is to test a strengths-based intervention to be delivered in a
primary care setting with adolescents and a parent. Investigators want to find out if the
intervention can help parents and teens communicate. Specifically Investigators want to see
if they can help parents and teens identify and build teen's strengths. Half the dyads will
receive the educational materials in conjunction with their teen's well-child visit, while
the other half will receive usual care at the well-child visit and receive the educational
materials at the end of the study. Additionally, Investigators expect that a strengths-based
intervention may also impact adherence to treatment in youth with a chronic illness. As such,
Investigators will include a subgroup of teenagers diagnosed with asthma in this study, to
assess whether the strengths-based intervention that the Investigators developed has an
impact on adherence.

Recent research suggests that parents and adolescents report an interest in doctors
facilitating increased parent-teen communication about teen strengths. However, little
research focuses on how to address this need in a primary care setting. Content from subject
matter experts along with data gathered from parents and teens were used to develop a novel
strengths-based intervention to be tested in primary care.

The study intervention being examined is called the Strengths Intervention Project and
includes a written pamphlet, a guided discussion activity, in-person/phone health coaching,
and in-person or mailed health care provider endorsement and key messaging. Measures will be
collected at baseline pre-intervention (T1), in clinic or over the phone at the time of the
intervention (T2), approximately two weeks post-intervention (T3), and approximately 2 months
post-intervention (T4). Daily diaries will also be utilized twice to gather data pre- and
post- intervention. We will measure feasibility of clinic implementation of intervention, as
well as influence of intervention on parent-teen communication and adolescent outcomes.

Adolescent Criteria:

Inclusion Criteria:

1. Teens age 13 to 15 years at the time of their upcoming well-child visit (Arm 1) OR
Teens age 13 to 15 years at the time of their last well-child visit (Arm 2)

2. Children's Hospital of Philadelphia (CHOP) primary care patient (Arm 1 and 2)

3. Scheduled for a well-child visit that parent and teen both plan to attend (Arm 1) OR
Attended a well-child visit with parent (Arm 2)

4. Diagnosed with Asthma > year (asthma subgroup; Arm 1 only)

5. Prescribed a controller medication year-round (asthma subgroup; Arm 1 only)

6. Adolescent has their own email account to complete electronic surveys (Arm 1 and 2)

Exclusion Criteria:

1. Not fluent in written or spoken English (Arm 1 and 2)

2. Attending a new patient well-child visit (Arm 1) OR attended a new patient well-child
visit (Arm 2)

3. Presence of developmental delay or pervasive developmental disorder that requires
special education services (Arm 1 and 2)

4. Psychiatric hospitalization of the adolescent in the past year (Arm 1 and 2)

5. Participated in studies: CHOP IRB # 15-011732 and/or CHOP IRB # 17-013895 (Arm 1 and
2)

6. Adolescent has sibling enrolled in (IRB 18-014922) (Arm 1 and 2)

Parent Criteria:

Inclusion Criteria:

1. Parent or legal guardian of a teen age 13 to 15 years at their upcoming well-child
visit at a CHOP primary care practice (Arm 1) OR Parent or legal guardian of a teen
age 13 to 15 years at their recent well-child visit at a CHOP primary care practice
(Arm 2)

2. Parent has their own email account to complete electronic surveys (Arm 1 and 2)

Exclusion Criteria:

1. Not fluent in written or spoken English (Arm 1 and 2)

2. Participated in studies: CHOP IRB # 15-011732 and/or CHOP IRB # 17-013895 (Arm 1 and
2)
We found this trial at
1
site
South 34th Street
Philadelphia, Pennsylvania 19104
 215-590-1000
Principal Investigator: Victoria A Miller, PhD
Phone: 267-425-1345
Children's Hospital of Philadelphia Since its start in 1855 as the nation's first hospital devoted...
?
mi
from
Philadelphia, PA
Click here to add this to my saved trials