Parenting Clinical Trial
— SIPOfficial title:
A Pilot Efficacy and Implementation Study of the Strengths Intervention Project
NCT number | NCT03496155 |
Other study ID # | 18-014922 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | May 4, 2018 |
Est. completion date | May 31, 2019 |
Verified date | October 2019 |
Source | Children's Hospital of Philadelphia |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 174 |
Est. completion date | May 31, 2019 |
Est. primary completion date | May 31, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 13 Years to 15 Years |
Eligibility |
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) |
Country | Name | City | State |
---|---|---|---|
United States | The Children's Hospital of Philadelphia | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Children's Hospital of Philadelphia | John Templeton Foundation |
United States,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Beliefs about Adolescents | 26 items (parents only); Likert scale (1= very unlikely; 7= very, very likely) | Baseline (T1) and 2-months (T4) | |
Primary | Change in Parent-Adolescent Communication (PACS) | 20 items (parent and teens); Likert scale (1= strongly disagree; 5= strongly agree) | Baseline (T1) and 2-months (T4) | |
Primary | Change in Confidence in exploring and using adolescent's strengths | 15 items (parents and teens); Likert scale (1=strongly disagree; 5= strongly agree) | Baseline (T1) and 2-months (T4) | |
Primary | Feasibility of consent rates | Feasibility will be demonstrated by consent rates =60% | 9 months | |
Primary | Feasibility of intervention implementation | Completion of core intervention components = 70%. | 1 month | |
Primary | Parent and adolescent acceptability of intervention materials | Adolescent and parent acceptability ratings =80%. Investigators will also elicit open-ended feedback. | 2-weeks post intervention (T3) | |
Primary | Parent and adolescent acceptability of intervention materials (additional) | 2 items (parents and teens); Yes/No/Not sure and Likert scale (1=very likely; 5 very unlikely) | 2-months post intervention (T4) | |
Primary | Provider acceptability of intervention | Provider acceptability ratings =80%. Investigators will also elicit open-ended feedback. | 9 months | |
Secondary | Change in Psychological well-being using the Flourishing Scale | Measure of psychological well-being. 8 items (parents and teens). (Likert scale 1= Strongly disagree; 2= Disagree; 3= Slightly disagree; 4= Mixed or neither agree nor disagree; 5= Slightly agree; 6= Agree; 7= Strongly agree). Score will be summed for range of 8 (Strong Disagreement with all items) to 56 (Strong Agreement with items). High scores signify that respondents view themselves in positive terms in important areas of functioning. | Baseline (T1) and 2-months (T4) | |
Secondary | Change in Adherence to inhaled controller medication use | 2-items about adherence to inhaled controller medication use (parent and teen) will be assessed using the Visual analog scale (0-10). | Baseline (T1) and 2-months (T4) |
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