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Mental Health ImpairmentSSC@KPC&PutnamNCT04069832

Evaluating the Single-Session Consultation Service at the Krasner Psychological Center and Putnam

A study testing Single-Session Consultation in people with Mental Health Impairment, run by Stony Brook University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Stony Brook University is home to several mental health clinics, that all work towards achieving overall wellness of their clients. The goals of Stony Brook University are met with the help of associated clinics that strive to improve wellness of individuals and their communities by helping to treat both mental and… Read more about this study

Who is it for?
Ages 13 years and older
Conditions the study is for
Mental Health Impairment
What is being tested?
Single-Session Consultation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteUnited States
Study dates
1 Oct 2019to 1 May 2020
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 13 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • All adolescent (ages 13+) and adult clients on the waitlist for clinical psychotherapy services at the KPC and MBCRC will be eligible to take part in this research.

Who cannot join

  • Child clients at the KPC and MBCRC under the age of 13 will not be eligible to participate in this study, because the Single-Session Consultation service presently being offered at the KPC and MBCRC is designed for use with adolescents and adults (i.e., it would be developmentally inappropriate for younger children.).
  • Non-English speaking individuals will not be eligible to receive any clinical services at the KPC and MBCRC because all therapists at the clinics are English-speaking.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Stony Brook University

    Stony Brook, New York, 11794-2500

Other trials in United States

About this study

Stony Brook University is home to several mental health clinics, that all work towards achieving overall wellness of their clients. The goals of Stony Brook University are met with the help of associated clinics that strive to improve wellness of individuals and their communities by helping to treat both mental and physical health impairments. Two of these many clinics are the Krasner Psychological Center (KPC), and the Mind Body Clinical Research Center (MBCRC)..

At present, the KPC and MBCRC face a challenge common to virtually all mental health clinics across the United States: the demand for psychological services far outpaces the number of available providers. Indeed, in the US, approximately 70% of those in need of mental health services do not receive them. As such, wait-lists at mental health clinics like the KPC and MBCRC are increasingly long, and longer wait-times for psychotherapy have predicted worse clinical outcomes once treatment is accessed (i.e., a 'nocebo' effect). Thus, there is a pressing need for effective, sustainable service delivery models that may facilitate more rapid access to care-for instance, providing a low-intensity service rapidly after an individual decides to seek treatment, capitalizing on client motivation. This sort of rapidly-provided, low-intensity service might have the added benefit of reducing overall waitlist lengths--e.g., if some subset of clients find the low-intensity service to be sufficient, a single session might be sufficient (in some cases) to spur positive behavioral and emotional change.

One solution to this problem is the integration of single-session services into mental health clinics. Extensive research suggests that both youths and adults can benefit from just one session of goal-directed counseling, and these clinical benefits have been observed for a wide array of problems-including anxiety, depression, self-harm, and interpersonal conflicts. This research suggests the possibility that, for some subset of clients, a single session of counseling may be helpful, or even sufficient, in reducing clinical distress. Therefore, the objective of this study is to examine the feasibility, acceptability, and short-term effects of the new Single-Session Consultation (SSC) service, which is presently being provided to clients on the waiting list for psychotherapeutic services at the Krasner Psychological Center and the Mind Body Clinical Research Center. The SSC offers clients the opportunity to participate in a single, goal-directed consultation session based on Solution-Focused Brief Therapy (SFBT) within two weeks of inquiring about services at the KPC and MBCRC (typically, clients wait 2-6 months prior to their initial clinic appointment). SFBT is an evidence-based therapy approach that guides services offered by existing single-session therapy clinics internationally. Clients who participate in the SSC at any of these clinics may find the session helpful; two weeks after participating in the session, they receive the option to remain on the waitlist for long-term psychotherapy or remove themselves from the waitlist for psychotherapy, depending on whether they feel their clinical needs have been successfully addressed.

Read the detailed description

The Stony Brook University (SBU) clinical psychology doctoral program is currently ranked 4th among the top clinical psychology doctoral programs in the country (2016, U.S. News and World Report, Best Graduate Schools) and is accredited by both the APA Committee on Accreditation (APA CoA) and the Psychological Clinical Science Accreditation System (PCSAS). The Krasner Psychological Center (KPC) is a psychology training clinic housed in the Department of Psychology and associated with the doctoral program in clinical psychology at SBU. The mission of the KPC is twofold, namely, (a) to provide high quality experiential training in the delivery of psychological services to trainees in the associated 3 doctoral program, as well as to externs, doctoral interns, and post-doctoral residents; and (b) to provide evidence-based mental health services to the nearby communities. All supervisors at the KPC are doctoral-level psychologists. Psychotherapy services at the KPC are based on Cognitive-Behavior Therapy models and include weekly, outpatient psychotherapy for a wide range of problems in children and adults; therapy is designed to be short-term, personalized, and effective in empowering clients to manage their symptoms and distress.

Similarly, the Mind Body Clinical Research Center (MBCRC) bases their interventions on evidence-based practices that address multiple factors associated with health impairments. Additionally, they focus on providing comprehensive psychiatric evaluations and assessments to aid in the creation of adequate treatment plans. The MBCRC specifically focuses on using mind-body to help identify risk and resiliency factors associated with mental health outcomes in their clients. This technique works in support of the scientific link that has been shown to exist between our mental/physical health with overall wellness and quality of life. Using this technique, the MBCRC is able to help individuals make changes early on that can help to prevent worsening symptomology of mental illness, preserve physical health, and make improvements in overall wellness.

The single-session consultation, a one-time service provided to adolescents and adults on the clinics' waitlist (which may extend from 2 to 6 months), includes components of Solution-Focused Brief Therapy (SFBT). SFBT lends itself naturally to the single-session format in that it focuses on the present and future, targeting the desired outcome of therapy, a future in which the primary problem is absent or less influential. Importantly, SFBT providers focus on the factors that maintain/underlie solutions rather than the factors than maintain/underlie problems.

GENERAL SCREENING PROCEDURES

When individuals seeking services at the KPC and MBCRC express interest in scheduling an appointment with a clinician, they are first instructed (by phone) about the clinical and research aims by the clinic's clinical research coordinator. The clinical research coordinator is a trained, independent staff member and is not involved in the provision of psychotherapy or single-session consultation services. The clinical research coordinator conducts a standardized, structured phone screen with the individual to identify primary reasons for seeking mental health services and to assess the appropriateness of presenting concerns for treatment at the KPC or MBCRC. If the individual is eligible to receive services at one of our clinics (i.e., if their concerns fall within the scope of clinical problems treated; if the individual/family is English-speaking; and if problems are not so acute as to require immediate hospitalization, in which case they are referred to the nearest emergency room), the client is placed on the waitlist for psychotherapy services.

During the same phone call, if the identified patient is 13 years or older, the clinical research coordinator then introduces the opportunity to participate in the Single Session Consultation (SSC) service at the KPC or MBCRC.

The clinical research coordinator indicates that as part of SSC service participation the client will be asked to complete questionnaires in order to provide their clinician with information about their current mental health, and for the purposes of planning and assessing the usefulness of services. The clinical research coordinator will also indicate that the individual may opt to allow or not allow us to use this data for research purposes. They will be informed that if they do choose to allow their data to be used for research, it will be de-identified and combined with other patient data for the purposes of understanding how well our treatment programs work for different types of individuals. The coordinator will emphasize that their choice to participate, or not participate in research will NOT impact their eligibility for the SSC service or longer-term psychotherapy in any way.

The clinical research coordinator will again review the purpose of the research study and obtain fully informed consent at the beginning of the patient's in-person intake visit. A private clinic room will be available for this purpose. Adult patients (or adolescent patient and her/his parent) can either agree or disagree to allow the research team to use their clinical data for research by checking the appropriate check-box on the paper consent form. Patients will also be able to elect to participate in the specific study described in the consent form and/or to have their de-identified data added to a registry for future unspecified research projects. Obtaining consent verbally by phone and in person at the initial intake visit will allow patients to ask questions and minimize the risk of coercion.

DATA COLLECTION PROCEDURES SPECIFIC TO THE SINGLE-SESSION CONSULTATION SERVICE

The following measures will be administered to clients immediately prior to participation in the SSC:

  • Brief Personal Data Questionnaire (Adult or Adolescent version)
  • State Hope Scale (assessing 'agency')
  • Brief Hopelessness Scale (assessing 'hope/hopelessness')
  • Brief Symptom Inventory - 18

Then, immediately following the one-hour SSC session, participants will be asked to complete immediate post-SSC questionnaires:

  • State Hope Scale (assessing 'agency')
  • Brief Hopelessness Scale (assessing 'hope/hopelessness')
  • Consultation Feedback Form

Finally, two weeks after completing the SSC, the clinical research coordinator will contact the client via phone to administer the Brief Symptom Inventory a second time. At the end of this phone call, the clinical research coordinator will then give the client the option to remain on the waitlist for long-term psychotherapy or remove themselves from the waitlist for psychotherapy, depending on whether they feel their clinical needs have been successfully addressed.

For therapists, "Therapist beliefs about SSC" measure will be administered before SSC training, immediately after SSC training, and two months after the SSC training date.

NOTE 1: A client may reschedule an SSC session if they are unable to attend it. The KPC and MBCRC will not limit the number of times a client is permitted to reschedule an SSC session, should they remain interested in receiving one. Additionally, if clients endorse significant clinical risk (to themselves or others) while participating in the study, study procedures may be interrupted (e.g., an SSC session may be terminated in order to address urgent clinical needs). If a client's initial SSC session is interrupted or terminated due to a need to address urgent clinical risk, the client will be permitted to reschedule their SSC session for a later date.

NOTE 2: If a participant does not respond to the clinic's requests for a 2-week follow-up phone call within two weeks of being contacted, per KPC and MBCRC policy, it will be assumed that the client is no longer interested in services and will be removed from the waiting list. Pre-to-post SSC data for these clients will still be used for analyses unless they request that their data not be used in the study.

NOTE 3: The lead investigator (Jessica Schleider) will train all SSC clinicians prior to their delivering SSC sessions with clients. This training will be approximately 2 hours in length and will review the principles and key elements of the SSC protocol, in addition to challenges that might emerge while delivering the SSC. The written SSC protocol used by clinicians in the study will be made publicly available by the Principal Investigator upon project completion.

Being tested
Single-Session Consultation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Single-Session ConsultationBehavioural

    Also called SSC

    A single, goal-directed consultation session based on Solution-Focused Brief Therapy (SFBT). SFBT is an evidence-based therapy approach that is primarily focused on the client's present problems and their immediate future. When using SFBT in a single-session the aim of the intervention becomes empowering the client to take the smallest possible steps towards their desired future.

Study groups in NCT04069832
Study groupRoleWhat they receive
InterventionOtherSINGLE-SESSION CONSULTATION
Receives: Behavioral: Single-Session Consultation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in State Hope Scale score ('agency')

    The State Hope Scale is a 6 item self-report measure of agentic, goal-directed thinking. Respondents rate 6 items on a Likert scale from 1 (definitely false) to 8 (definitely true). Higher mean scores reflect a greater sense of personal agency (i.e., personal capacity to pursue and sense of having attained goals). Scores range from 1-8.

    Measured: Pre-Single-Session Consultation (SSC) & immediately Post-SSC (1-3 minutes post-intervention))

  2. Change in Beck Hopelessness Scale - 4 item version score ('hope')

    Respondents report agreement with 4 items, each rated on a 0-3 scale, indicating levels of hopelessness about the future. Higher summed scores reflect greater levels of hopelessness, and scores range from 0-12.

    Measured: Pre-Single-Session Consultation (SSC) & immediately Post-SSC (1-3 minutes post-intervention))

Secondary outcomes (3)
  1. Change in Brief Symptom Inventory-18

    The Brief Symptom Inventory-18 (BSI-18) assesses self reported psychopathology and distress. Respondents rate endorsement of 18 physical and emotional complaints on a 0-4 Likert scale. The total sum score yields an additional total distress score (range: 0-72). Higher scores indicate higher levels of overall psychological distress.

    Measured: Pre-SSC & 2 week follow-up

  2. Consultation Feedback Form

    The consultation feedback form contains 5 items, rated on a 1 ("Not at all") to 5 ("Very much") Likert scale, indicating endorsement of a series of statements about responses to the Single Session Consultation program (e.g., "Did you find the consultation helpful in addressing your concern(s)?" and "How hopeful are you that the action plan will be useful?." Higher mean scores across these 5 items indicates greater perceived usefulness of the SSC.

    Measured: Immediately Post-SSC (1-3 minutes post-intervention) only

  3. Therapist Beliefs about SSC

    A brief measure examining therapists' perceived acceptability, feasibility, and effectiveness of the Single Session Consultation (SSC) program. The measure is comprised of questions rated on a 1 ("Completely Disagree") to 5 ("Completely Agree") scale, indicating endorsement of a series of statements about the Single Session Consultation Program, and short answer questions. Higher mean scores across these 5 items indicate greater perceived acceptability, feasibility, and effectiveness of the SSC. This measure will be administered to clinicians at Mind Body Research Center and Adolescent Outpatient Psychiatry only due to the delayed addition of this measure.

    Measured: Pre-SSC Training, Immediately post-SSC training, and 2 months after SSC training

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Aug 2019
  2. Study start1 Oct 2019
  3. Primary completion30 Apr 2020
  4. Study completion1 May 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04069832
Sponsor's protocol ID
IRB2019-00362
Acronym
SSC@KPC&Putnam
Status last verified
May 2020
First submitted
21 Aug 2019
Last updated
29 May 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: De-identified participant-level data will be made available on Open Science Framework upon conclusion of the pilot study (N= 60).

Questions about this trial

What is this clinical trial studying?

A study testing Single-Session Consultation in people with Mental Health Impairment, run by Stony Brook University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 29 May 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in State Hope Scale score ('agency') (time frame: Pre-Single-Session Consultation (SSC) & immediately Post-SSC (1-3 minutes post-intervention))). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 May 2020.

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