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Clinical Trials/NCT01750892
NCT01750892CompletedNot Applicable

Transition From Pediatric to Adult Services: A Primary Care Based Model for Patients With Chronic Conditions

Children's Hospital of Philadelphia1 site in 1 country43 target enrollmentStarted: October 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
43
Locations
1
Primary Endpoint
Successful transition to an adult provider

Study Overview

Brief Summary

This study is looking at ways to help young people with chronic health conditions take better care of their health and find an adult doctor.

Detailed Description

The purpose of this study is to determine whether providing targeted transition-related skills through interventions with varying degrees of intensity (from the low intensity Basic intervention group, to the mild intensity Group Intervention group, to the high intensity Full Intervention group) results in improved transition readiness and self-care skills and improved successful transition to adult-based services for young adults with chronic health conditions. Secondary objectives include determining if the transition interventions enhance transition-related satisfaction among participants, their caregivers and the involved pediatric and adult providers.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
19 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Young Adult Inclusion Criteria:
  • •Males or females age 19 years of age or older
  • •Presence of at least 1 Chronic Condition and/or Cognitive Disability
  • •Last visit with pediatric primary care provider occurring on or after January 1, 2011
  • •Currently active in one of four identified pediatric practices (Cobbs Creek, Chestnut Hill, Market Street, West Chester)
  • •Current primary care provider approval for participation
  • •English speaking
  • •Young Adult

Exclusion Criteria

  • •Male or female age < 19 years
  • •No presence of a chronic condition or cognitive disability
  • •Last visit with pediatric PCP occurring prior to January 1, 2011
  • •Not currently active in one of four identified pediatric practices (Cobbs Creek, Chestnut Hill, Market Street, West Chester)
  • •Current PCP disapproves participation
  • •Non-English speaking
  • •Caregiver Inclusion Criteria:
  • •Has a child enrolled in the study
  • •Child has consented/assented to allow them to participate
  • •English speaking
  • •Caregiver Exclusion Criteria:
  • •Child did not consent/assent to allow them to participate
  • •Non-English speaking

Arms & Interventions

Group 1: Control

Active Comparator

Group 1 will be the control group. They will complete questionnaires but will otherwise receive usual care from their Primary Care Provider (PCP). At the end of the study period they will be given the Study Materials for participating.

Intervention: Study Materials (Other)

Group 3: Group Intervention

Experimental

Group 3 (Group Intervention) will receive the Study Materials at the beginning of the study and will also be invited to attend two REACH for Independence group sessions.

Intervention: REACH for Independence (Behavioral)

Group 3: Group Intervention

Experimental

Group 3 (Group Intervention) will receive the Study Materials at the beginning of the study and will also be invited to attend two REACH for Independence group sessions.

Intervention: Study Materials (Other)

Group 4: Full Intervention

Experimental

Group 4 (Full Intervention) will receive the Study Materials at the beginning of the study, will be invited to attend the REACH for Independence group sessions, and will be invited to a Transition Consult with an MD and social worker.

Intervention: Transition Consult (Behavioral)

Group 4: Full Intervention

Experimental

Group 4 (Full Intervention) will receive the Study Materials at the beginning of the study, will be invited to attend the REACH for Independence group sessions, and will be invited to a Transition Consult with an MD and social worker.

Intervention: Study Materials (Other)

Group 4: Full Intervention

Experimental

Group 4 (Full Intervention) will receive the Study Materials at the beginning of the study, will be invited to attend the REACH for Independence group sessions, and will be invited to a Transition Consult with an MD and social worker.

Intervention: REACH for Independence (Behavioral)

Group 2: Basic Intervention

Experimental

Group 2 (Basic Intervention) will receive the Study Materials at the beginning of the study but will otherwise continue with their usual PCP care.

Intervention: Study Materials (Other)

Outcomes

Primary Outcomes

Successful transition to an adult provider

Time Frame: 10 months

The primary outcome is successful transition to an adult provider, as evidenced by at least 1 visit with an adult provider within 10 months of the baseline visit.

Secondary Outcomes

  • Increased self-care and transition related skills(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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