CClinicalTrials.gg
WithdrawnNCT06614842Updated Jun 18, 2026

Common Factors Group Psychotherapy for General Mental Health Concerns

An interventional study of Common Factors Group Psychotherapy in Major Depression, Generalized Anxiety and Stress Disorder, Post Traumatic, sponsored by University of Alabama at Birmingham. Withdrawn. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-06-18.

Sponsored by University of Alabama at Birmingham · Not applicable, Interventional, and Treatment

Why this study was withdrawn
Inability for consistent recruitment.
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Major Depression
  • Generalized Anxiety
  • Stress Disorder, Post Traumatic
  • Stress
  • Mental Disorders

Keywords

  • common factors psychotherapy
03

In context

Depressive Disorder, Major

2,741 studies on the registry are indexed under Depressive Disorder, Major; 559 are open to participants now.

Browse Depressive Disorder, Major studies →

Lead sponsor

University of Alabama at Birmingham is the lead sponsor of 1,396 studies on the registry; 284 are open to participants now.

Of its 156 completed or terminated interventional studies of FDA-regulated products, 124 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • At least 18 years old
  • Experiencing self-reported psychological distress

Exclusion criteria

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)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • 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)

    Behavioral: Common Factors Group Psychotherapy

Interventions

  • BehavioralCommon Factors Group Psychotherapy

    This intervention will not contain active ingredients from established specific forms of psychotherapy (e.g., cognitive-behavioral therapy, dialectical behavioral therapy)

06

What researchers measure

Primary outcomes

  1. Generalized Anxiety Disorder-7 Screener

    Measure of anxiety symptoms. High scores more symptoms.

    Time frame: At enrollment and at the end of treatment at 6 weeks

  2. Patient Health Questionnaire-9 Screener

    Measure of depressive symptoms. High scores more symptoms.

    Time frame: At enrollment and at the end of treatment at 6 weeks

  3. Patient Checklist-5

    Measure of post-traumatic stress symptoms. High scores more symptoms.

    Time frame: At enrollment and at the end of treatment at 6 weeks

  4. Yale-Brown Obsessive Compulsive Scale

    Measure of obsessive compulsive disorder symptoms. High scores more symptoms.

    Time frame: At enrollment and at the end of treatment at 6 weeks

  5. Alcohol Use Disorders Identification Test

    Measure of concerning alcohol use. High scores more symptoms.

    Time frame: At enrollment and at the end of treatment at 6 weeks

  6. National Institute of Drug Abuse Modified Alcohol, Smoking, and Substance Involvement Screening Test

    Measure of substance use. High scores more use.

    Time frame: At enrollment and at the end of treatment at 6 weeks

Secondary outcomes

  1. Life Quality Scale

    Measure of life quality. High scores better life quality.

    Time frame: At enrollment and at the end of treatment at 6 weeks

  2. Experiential Avoidance Rating Scale

    Measure of experiential avoidance. High scores more symptoms.

    Time frame: At enrollment and at the end of treatment at 6 weeks

Other outcomes

  1. Therapeutic Alliance Scale

    Measure of patient-therapist alliance during therapy. High scores better alliance.

    Time frame: At conclusion of therapy after 6 weeks.

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Yes — All de-identified data collected will be available2

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06614842
Lead sponsor
University of Alabama at Birmingham
Responsible party
Nicholas C. Borgogna (Assistant Professor, University of Alabama at Birmingham) — Principal investigator
First posted
Sep 26, 2024
Start date
Jan 17, 2025
Primary completion
Dec 30, 2025
Completion
Dec 30, 2025
Last update
Jun 18, 2026

Study contacts

Nicholas Borgogna, PhD
principal investigator · University of Alabama at Birmingham
Drew Whittington, MS, MA
principal investigator · University of Alabama at Birmingham

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion