NCT03255954

Brief Summary

Interpersonal Counseling (IPC) is brief, structured modification of Interpersonal Psychotherapy (IPT). IPC was developed as a brief triage manual to treat depression in primary care, family practice and non-mental health programs, and work and educational settings. College and university students are at the age where first episodes of depression, bipolar disorder, or psychosis may occur. IPC is relevant for this population as many university students' distress are related to profound life changes, role transitions, loneliness and social/cultural isolation, which are focuses of treatment in IPC. While there is considerable evidence for the efficacy of IPT and IPC, this adaptation for university students has not yet been studied. The investigators propose to administer IPC to across several college campuses, and to recruit 20 participants at each counseling center. Participants will receive 3-6 one-hour therapy sessions, and will complete self-report measures of depression, psychosocial functioning, college adjustment, and treatment satisfaction. IPC has the potential to reduce depressive symptoms and prevent presenting symptoms from worsening. For these reasons, developing and testing a brief, yet comprehensive psychosocial intervention for distressed college students has tremendous importance.

Trial Health

90
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
42

participants targeted

Target at P25-P50 for not_applicable depression

Timeline
Completed

Started Feb 2017

Longer than P75 for not_applicable depression

Geographic Reach
2 countries

3 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 10, 2017

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

May 23, 2017

Completed
3 months until next milestone

First Posted

Study publicly available on registry

August 21, 2017

Completed
6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 30, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2023

Completed
Last Updated

September 7, 2023

Status Verified

September 1, 2023

Enrollment Period

6.6 years

First QC Date

May 23, 2017

Last Update Submit

September 6, 2023

Conditions

Keywords

Interpersonal Counseling

Outcome Measures

Primary Outcomes (1)

  • Retention rate

    Retention rate will be assessed by calculating the number of participants who completed the study compared to the number of participants who enrolled in the study

    One year

Secondary Outcomes (1)

  • Satisfaction questionnaire

    Participants complete a satisfaction questionnaire when they have completed the study (maximum of 3 months)

Study Arms (1)

Interpersonal Counseling-C

EXPERIMENTAL

Interpersonal Counseling for University Counseling Centers is a psychotherapeutic intervention

Other: Interpersonal Counseling for University Counseling Centers

Interventions

Interpersonal Counseling (IPC) is a brief version of Interpersonal Psychotherapy (IPT). IPC synthesizes the fundamental IPT principles into 3-6 sessions. Individuals receiving IPC are initially assessed for symptoms of depression, and then encouraged to identify interpersonal problem areas which may be contributing to their presenting symptoms.

Also known as: IPC-C
Interpersonal Counseling-C

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • years old
  • Currently receiving counseling at one of the study locations
  • Adjustment disorder with depressed mood or mild to moderate depression which correlates with a Patient Health Questionnaire-9 (PHQ-9) score of 5-14.

You may not qualify if:

  • Pregnancy.
  • Non-English speaking
  • Poses a significant risk for dangerousness to self or others, or suffers from a concomitant medical or psychiatric comorbidity that makes the study protocol inadvisable (i.e., post-traumatic stress disorder, autism, psychotic disorder, bipolar I or II disorder, eating disorder, alcohol or substance abuse or current use)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

Homewood Counseling Center

Baltimore, Maryland, 21218, United States

Location

Amherst College Counseling Center

Amherst, Massachusetts, 01002, United States

Location

University of Toronto

Toronto, Canada

Location

MeSH Terms

Conditions

Depression

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Study Officials

  • Leslie Miller, MD

    Johns Hopkins University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 23, 2017

First Posted

August 21, 2017

Study Start

February 10, 2017

Primary Completion

August 30, 2023

Study Completion

August 30, 2023

Last Updated

September 7, 2023

Record last verified: 2023-09

Data Sharing

IPD Sharing
Will not share

Locations