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

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

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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