Implementation of Transdx Group for POTS

Completed · Not applicable

Conditions studied: Dysautonomia, Anxiety, Depression

In brief

The proposed intervention is focused on developing and implementing a psychological approach incorporated into a group-based outpatient intervention for pediatric autonomic dysfunction. The investigators hypothesize that their intervention will result in improvements in the transdiagnostic mechanisms specifically targeted by components of their intervention including sleep, information processing, and youth/parent experiential avoidance.

Key facts

Study ID

NCT03185247

Run by

University of Colorado, Denver

People needed

16

Starts

2017-05-26

Expected to finish

2019-09-01

Last updated by the study team

2019-09-26

Who can join

Age: 13 and older, up to 18. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Adolescent participants must be
• between the ages of 13-18 years old,
• english speaking, and
• have been diagnosed with autonomic dysfunction, dysautonomia, orthostatic intolerance, and/or POTS.
• Participants must also:
• endorse symptoms of autonomic dysfunction on the COMPASS 31 (measures are described below), and show
• moderate functional impairment, and/or
• some psychiatric symptoms in the domains of anxiety and/or depression.
• FDI scores must be greater than 12 (see Kashikar-Zuck et al., 2011 for an empirical rationale).
• Must have attended at least one day of school per week during the past month.
• On the measures of anxiety (SCARED) and depression (CDI), the adolescent's scale score must be above the "average" range based on T scores (CDI) or within the "clinical" range (SCARED).
• Each participant must have at least one English-speaking parent/legal guardian who can provide informed consent for the adolescent, as well as participate in the study.
• Each adolescent and their parent/legal guardian(s) must be English-speaking.

You may not qualify if…

• Adolescent participants;
• wards of the state,
• endorse active homicidal or suicidal ideation,
• have an intellectual disability, a pervasive developmental disability or significant developmental delay,
• endorse an active substance use disorder, and
• are currently participating in individual or group psychotherapy.
• do not have in-network health insurance that covers Health and Behavior interventions, or
• are unable to self-pay.
• Parent/legal guardian(s) are
• unwilling to participate in the study,
• are non-English speaking, or
• have an intellectual disability, a pervasive developmental disability or significant developmental delay, and/or
• do not have legal custody of the adolescent participant.

Where it is running

• Children's Hospital Colorado — Aurora, Colorado, United States

Full record on ClinicalTrials.gov

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