search
Back to results

Family Centered Advanced Care Planning for Adolescents With HIV/AIDS and Their Families

Primary Purpose

HIV Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Family Centered Advanced Care Planning (FCACP) sessions
Health education control sessions
Sponsored by
Maureen Lyon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Quality of Life, Adolescent, Advance Care Planning, Palliative Care, End-of-Life Care, HIV/AIDS, Psychological Adjustment

Eligibility Criteria

12 Years - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Adolescent Eligibility Criteria:

  • Diagnosed with HIV/AIDS
  • Between the ages of 14 and 21 years
  • Aware of his or her HIV status
  • Able to speak English
  • Intelligence Quotient (IQ) greater than 69 (all patients have IQ testing results in chart as part of standard of care)
  • Consent from the legal guardian if between ages of 14 and 17
  • Consent from the surrogate if between ages of 18 and 21
  • Assent from adolescent aged 14 to 17
  • Consent from adolescent aged 18 to 21

Legal Guardian Eligibility Criteria (for guardians of adolescents aged 14 to 17):

  • Adolescent is willing to discuss problems related to HIV with him/her
  • Age 21 or older
  • Able to speak English
  • Legal guardian

Surrogate Eligibility Criteria:

  • Selected by adolescent aged 18 to 21
  • Age 21 or older
  • Willing to discuss problems related to HIV and EOL
  • Able to speak English

Exclusion Criteria For All Participants:

  • Depression in the moderate to severe range on Beck Depression Inventory
  • Unaware of HIV status of self, or if proxy, of adolescent
  • Presence of HIV dementia, determined at screening using the HIV Dementia Scale
  • Active homicidality or suicidality, determined at baseline screening by psychologist or researcher

Sites / Locations

  • Children's Research Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

A

B

Arm Description

Participants will receive three 60- to 90-minute health education control sessions.

Participants will receive three 60- to 90-minute Family Centered Advanced Care Planning sessions.

Outcomes

Primary Outcome Measures

Improved mental health outcomes (e.g., decreased anxiety, depression), improved quality of life, and improved plans and actions (e.g., communication with primary health care provider, an advanced directive in the medical chart)

Secondary Outcome Measures

Improved congruence about end-of-life care between adolescents and family, using the Statement of Treatment Preferences

Full Information

First Posted
July 25, 2008
Last Updated
May 19, 2015
Sponsor
Maureen Lyon
Collaborators
National Institute of Mental Health (NIMH)
search

1. Study Identification

Unique Protocol Identification Number
NCT00723476
Brief Title
Family Centered Advanced Care Planning for Adolescents With HIV/AIDS and Their Families
Official Title
Family Centered Advanced Care Planning (FCACP)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Completed
Study Start Date
September 2005 (undefined)
Primary Completion Date
August 2008 (Actual)
Study Completion Date
September 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Maureen Lyon
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will examine the efficacy of Family Centered Advance Care Planning in enhancing quality of life, integrating effective end-of-life care, and preventing depression and anxiety among HIV infected adolescents and their family members.
Detailed Description
More than 30,000 adolescents in the United States die annually from the effects of chronic illnesses. The anxiety from facing a terminal illness often hinders adolescents in making decisions about their own end-of-life (EOL) care. Although minors' preferences are not legally binding, legislature, research, and professional guidelines all recommend that adolescent patients become involved in EOL decisions as part of routine intervention while they are stable. Family Centered Advance Care Planning (FCACP) is an intervention that facilitates EOL discussion among adolescents, their families, and their care providers. This pilot study will examine FCACP's effects on adaptive coping, psychological adjustment, quality of life, and plans and actions in HIV infected adolescents. The study will also provide feedback used for improving the FCACP Web site. This study will include HIV or AIDS infected adolescents ranging in age from 14 to 21 who will jointly enroll with a selected surrogate older than 21. The adolescent/surrogate pairs will be randomly assigned to receive either the FCACP intervention or a health education control intervention. Pairs not immediately ready to participate will form an observational group. Pairs in the FCACP group will meet with a trained facilitator weekly for a 60- to 90-minute session for a total of 3 weeks. During the first session, participants will take the Lyon Advance Care Planning Survey. The second session will consist of the Respecting Choices Interview, where patients will discuss treatment preferences. The Family Problem-Solving session will be last, culminating with the patient's completion of an advance directive. The control groups will follow the same meeting schedule, but will receive health education sessions, not FCACP sessions. Standardized self-report measures will be administered upon entry, after completion of the sessions, and at a 3-month follow up. Usage data will also be analyzed regarding feasibility and acceptability of FCACP as a standard treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Quality of Life, Adolescent, Advance Care Planning, Palliative Care, End-of-Life Care, HIV/AIDS, Psychological Adjustment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
82 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Active Comparator
Arm Description
Participants will receive three 60- to 90-minute health education control sessions.
Arm Title
B
Arm Type
Experimental
Arm Description
Participants will receive three 60- to 90-minute Family Centered Advanced Care Planning sessions.
Intervention Type
Behavioral
Intervention Name(s)
Family Centered Advanced Care Planning (FCACP) sessions
Intervention Description
FCACP will include three 60- to 90-minute weekly sessions. Sessions consisting of structured conversations with HIV infected adolescents, their proxies, and trained facilitators will aim to enhance quality of life by integrating effective end-of-life (EOL) care and minimizing depression and anxiety. The three sessions will consist of a structured EOL survey, an FCACP interview, and a family problem-solving lesson.
Intervention Type
Behavioral
Intervention Name(s)
Health education control sessions
Intervention Description
Health education control sessions will include three 60- to 90-minute sessions and will involve adolescents with HIV/AIDS and their proxies. Topics covered during sessions will include developmental history, planning for the future, and safety tips.
Primary Outcome Measure Information:
Title
Improved mental health outcomes (e.g., decreased anxiety, depression), improved quality of life, and improved plans and actions (e.g., communication with primary health care provider, an advanced directive in the medical chart)
Time Frame
Measured at Month 3 of follow-up
Secondary Outcome Measure Information:
Title
Improved congruence about end-of-life care between adolescents and family, using the Statement of Treatment Preferences
Time Frame
Measured immediately post-treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Adolescent Eligibility Criteria: Diagnosed with HIV/AIDS Between the ages of 14 and 21 years Aware of his or her HIV status Able to speak English Intelligence Quotient (IQ) greater than 69 (all patients have IQ testing results in chart as part of standard of care) Consent from the legal guardian if between ages of 14 and 17 Consent from the surrogate if between ages of 18 and 21 Assent from adolescent aged 14 to 17 Consent from adolescent aged 18 to 21 Legal Guardian Eligibility Criteria (for guardians of adolescents aged 14 to 17): Adolescent is willing to discuss problems related to HIV with him/her Age 21 or older Able to speak English Legal guardian Surrogate Eligibility Criteria: Selected by adolescent aged 18 to 21 Age 21 or older Willing to discuss problems related to HIV and EOL Able to speak English Exclusion Criteria For All Participants: Depression in the moderate to severe range on Beck Depression Inventory Unaware of HIV status of self, or if proxy, of adolescent Presence of HIV dementia, determined at screening using the HIV Dementia Scale Active homicidality or suicidality, determined at baseline screening by psychologist or researcher
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maureen E. Lyon, PhD
Organizational Affiliation
Children's Research Institute and Children's National Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Research Institute
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20010
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
19327074
Citation
Lyon ME, Garvie PA, Briggs L, He J, McCarter R, D'Angelo LJ. Development, feasibility, and acceptability of the Family/Adolescent-Centered (FACE) Advance Care Planning intervention for adolescents with HIV. J Palliat Med. 2009 Apr;12(4):363-72. doi: 10.1089/jpm.2008.0261.
Results Reference
background
PubMed Identifier
22096382
Citation
Lyon ME, Garvie PA, Briggs L, He J, Malow R, D'Angelo LJ, McCarter R. Is it safe? Talking to teens with HIV/AIDS about death and dying: a 3-month evaluation of Family Centered Advance Care (FACE) planning - anxiety, depression, quality of life. HIV AIDS (Auckl). 2010;2:27-37. doi: 10.2147/hiv.s7507. Epub 2010 Feb 18.
Results Reference
background
PubMed Identifier
22771129
Citation
Garvie PA, He J, Wang J, D'Angelo LJ, Lyon ME. An exploratory survey of end-of-life attitudes, beliefs, and experiences of adolescents with HIV/AIDS and their families. J Pain Symptom Manage. 2012 Sep;44(3):373-85.e29. doi: 10.1016/j.jpainsymman.2011.09.022. Epub 2012 Jul 7.
Results Reference
background
PubMed Identifier
23104266
Citation
Lyon ME, Garvie P, He J, Malow R, McCarter R, D'Angelo LJ. Spiritual well-being among HIV-infected adolescents and their families. J Relig Health. 2014 Jun;53(3):637-53. doi: 10.1007/s10943-012-9657-y.
Results Reference
background
PubMed Identifier
19171571
Citation
Lyon ME, Garvie PA, McCarter R, Briggs L, He J, D'Angelo LJ. Who will speak for me? Improving end-of-life decision-making for adolescents with HIV and their families. Pediatrics. 2009 Feb;123(2):e199-206. doi: 10.1542/peds.2008-2379.
Results Reference
result

Learn more about this trial

Family Centered Advanced Care Planning for Adolescents With HIV/AIDS and Their Families

We'll reach out to this number within 24 hrs