- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06614842
Common Factors Group Psychotherapy for General Mental Health Concerns
December 29, 2025 updated by: Nicholas C. Borgogna, University of Alabama at Birmingham
The current research will investigate the impact of general psychotherapy using common factors (i.e., techniques and communication skills that are common to all major forms of psychotherapy) to investigate whether mental health professionals can treat a variety of mental health concerns utilizing this general form of psychotherapy as opposed to specific forms of psychotherapy that may require specific trainings or education.
Study Overview
Status
Withdrawn
Conditions
Intervention / Treatment
Detailed Description
The current research will investigate the impact of general psychotherapy using common factors (i.e., techniques and communication skills that are common to all major forms of psychotherapy) to investigate whether mental health professionals can treat a variety of mental health concerns utilizing this general form of psychotherapy as opposed to specific forms of psychotherapy that may require specific trainings or education.
Study Type
Interventional
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Alabama
-
Birmingham, Alabama, United States, 35233
- University of Alabama at Birmingham
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- At least 18 years old
- Experiencing self-reported psychological distress
Exclusion Criteria:
- has engaged in self-harm within the last three months
- has attempted suicide within the last year
- has had an active plan to attempt suicide within the last 30 days
- currently diagnosed with any eating disorder
- has experienced hallucinations or delusions within the last 30 days
- has used narcotics within the last 7 days (heroin, meth, crack cocaine, opioids)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Common Factors Group Therapy
We will use a general common factors psychotherapy utilizing only psychotherapeutic techniques common to most forms of psychotherapy (e.g., listening and communication skills)
|
This intervention will not contain active ingredients from established specific forms of psychotherapy (e.g., cognitive-behavioral therapy, dialectical behavioral therapy)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Generalized Anxiety Disorder-7 Screener
Time Frame: At enrollment and at the end of treatment at 6 weeks
|
Measure of anxiety symptoms.
High scores more symptoms.
|
At enrollment and at the end of treatment at 6 weeks
|
|
Patient Health Questionnaire-9 Screener
Time Frame: At enrollment and at the end of treatment at 6 weeks
|
Measure of depressive symptoms.
High scores more symptoms.
|
At enrollment and at the end of treatment at 6 weeks
|
|
Patient Checklist-5
Time Frame: At enrollment and at the end of treatment at 6 weeks
|
Measure of post-traumatic stress symptoms.
High scores more symptoms.
|
At enrollment and at the end of treatment at 6 weeks
|
|
Yale-Brown Obsessive Compulsive Scale
Time Frame: At enrollment and at the end of treatment at 6 weeks
|
Measure of obsessive compulsive disorder symptoms.
High scores more symptoms.
|
At enrollment and at the end of treatment at 6 weeks
|
|
Alcohol Use Disorders Identification Test
Time Frame: At enrollment and at the end of treatment at 6 weeks
|
Measure of concerning alcohol use.
High scores more symptoms.
|
At enrollment and at the end of treatment at 6 weeks
|
|
National Institute of Drug Abuse Modified Alcohol, Smoking, and Substance Involvement Screening Test
Time Frame: At enrollment and at the end of treatment at 6 weeks
|
Measure of substance use.
High scores more use.
|
At enrollment and at the end of treatment at 6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Life Quality Scale
Time Frame: At enrollment and at the end of treatment at 6 weeks
|
Measure of life quality.
High scores better life quality.
|
At enrollment and at the end of treatment at 6 weeks
|
|
Experiential Avoidance Rating Scale
Time Frame: At enrollment and at the end of treatment at 6 weeks
|
Measure of experiential avoidance.
High scores more symptoms.
|
At enrollment and at the end of treatment at 6 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Therapeutic Alliance Scale
Time Frame: At conclusion of therapy after 6 weeks.
|
Measure of patient-therapist alliance during therapy.
High scores better alliance.
|
At conclusion of therapy after 6 weeks.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Nicholas Borgogna, PhD, University of Alabama at Birmingham
- Principal Investigator: Drew Whittington, MS, MA, University of Alabama at Birmingham
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 17, 2025
Primary Completion (Actual)
December 30, 2025
Study Completion (Actual)
December 30, 2025
Study Registration Dates
First Submitted
September 24, 2024
First Submitted That Met QC Criteria
September 24, 2024
First Posted (Actual)
September 26, 2024
Study Record Updates
Last Update Posted (Actual)
January 5, 2026
Last Update Submitted That Met QC Criteria
December 29, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB-300013539
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
All de-identified data collected will be available2
IPD Sharing Time Frame
When results are published
IPD Sharing Access Criteria
Requesting researchers
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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