Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT04010747 |
Other study ID # |
H-41305 |
Secondary ID |
5K23MH118373-042 |
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
March 1, 2020 |
Est. completion date |
April 30, 2022 |
Study information
Verified date |
April 2023 |
Source |
Boston Medical Center |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
The study population for this research will include parents and concerned significant others
(PCSO) of individuals experiencing recent (past five years) onset of a psychotic disorder
(hereafter referred to as individuals with psychosis, "IP") who are not currently engaged
with, or at risk for disengagement from, treatment. MILO is a brief and structured
intervention that teaches motivational interviewing communication strategies. The initial aim
(phase 1) of this pilot study is to evaluate feasibility of the intervention. The secondary
aims are to evaluate the effectiveness of MILO for (1) enhancing the engagement of IP with
evidence-based treatments and (2) reducing distress among PCSO. The investigators hypothesize
that the intervention will be superior to control condition for both enhancing IP engagement
with mental health services and reducing PCSO distress.
Description:
First Episode Psychosis (FEP) often represents a time of crisis for young people and their
families. Since peak onset occurs during late adolescence and early adulthood, the onset of
serious mental health challenges can disrupt plans for education, relationships, and other
milestones of independence. Although some psychoses are brief and self-limiting, more often
these symptoms portend a potentially chronic and disabling psychiatric disorder such as
schizophrenia. FEP can also be acutely dangerous: youth with FEP are far more likely to die
in the year following their diagnosis relative to the general population of 16-30 year old's
in the United States. Approximately 100,000 youth in the United States experience FEP every
year. Young people identified by providers as experiencing FEP often slip through the cracks
before they reach appropriate treatment. A review of privately insured adolescents and young
adults in the US showed that 62% of young people in the US with FEP filled no outpatient
prescriptions, and 41% received no outpatient psychotherapy, in the year following their
index diagnosis. Among those who do have an initial encounter with specialized FEP outpatient
care, high attrition is a common problem, with 30% of individuals initially enrolled in first
episode programs dropping out prior to completing treatment.
Many individuals experiencing psychosis are reluctant to seek mental health treatment due to
lack of insight and fear of psychiatric interventions. Young adults may be torn between
distress and dissatisfaction relating to their symptoms and functioning, and mistrust of
mental health providers and irritation with their parents' concern. Motivational Interviewing
(MI) techniques are designed to elicit this ambivalence through nonjudgmental listening, so
that discrepancies between current behaviors and ideal outcomes can be explored.
Clinician-delivered MI has been identified as effective for enhancing adherence once
individuals with psychosis are involved in care, and may also be useful for engaging those
who are not yet interested in treatment. Several studies have found positive results in
training and deploying non-professionals to use MI to influence others' health behaviors. MI
training for parents and concerned significant others (PCSO) is a promising venue through
which PCSO can specifically influence their loved one's decision to seek care and adhere to
treatment plans.
MILO is a structured and goal oriented intervention that seeks to accomplish two aims. The
primary aim is to facilitate the engagement of IP with evidence-based treatments. The
secondary aim is to reduce the distress and increase the wellbeing of PCSO. The intervention
will be trialed for feasibility (phase 1, n = 30) and then tested against a small "treatment
as usual" (TAU) control arm (phase 2, n = 40). During phase 2, participants will be randomly
assigned to either receive MILO (50%) or TAU (50%). The trial will involve a total of 70
participants.