Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07208851

Development, Feasibility, and Acceptability of a One-time Problem Management Plus (PM+) Booster Session in the Bahamas: A Pilot Randomized Controlled Trial

Led by The New School · Updated on 2026-01-06

50

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the development, feasibility, and acceptability of a one-time booster session for Problem Management Plus (PM+), a World Health Organization behavioral intervention. This pilot randomized controlled trial focuses on adults in Grand Bahama experiencing mild to moderate depression and anxiety symptoms. The study aims to support mental health by enhancing the existing PM+ program, delivered by trained local therapists at the Grand Bahama Resilience Center (GBRC). The study includes three phases: training GBRC counselors in PM+, collaboratively creating a one-time booster session, and conducting a pilot trial with 50 adult clients. Participants first receive five individual PM+ sessions focusing on skills like diaphragmatic breathing and problem management. After completing PM+, participants are randomly assigned either to receive a booster session three months later or to a control group receiving a reminder phone call. The booster session reviews PM+ strategies and helps develop future plans. Participants complete self-report surveys before PM+, one week after, at three months, and six months post-treatment. Researchers assess anxiety and depression levels, functioning, and psychological outcomes using validated scales such as the Hospital Anxiety and Depression Scale and PHQ-9. Qualitative interviews with participants and providers provide deeper insight into intervention acceptability. The study spans approximately 6 to 7 months per participant, with ongoing monitoring and evaluation to inform future mental health support programs.

CONDITIONS

Brief Title

Developing a Booster Session for Problem Management Plus in the Bahamas: A Pilot Randomized Controlled Trial

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults of 18 years or above
  • English-speaking
  • A score of less than 91 on Global Assessment of Functioning
  • Located in the Bahamas
Not Eligible

You will not qualify if you...

  • Imminent suicide risk assessed by Columbia Suicide Severity Rating Scale
  • Severe mental disorder such as psychotic disorders
  • Severe cognitive impairment such as severe intellectual disability or dementia

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) for screening and informed consent

Treatment

Duration - Approximately 6 to 8 weeks

Participants receive the full 5-session Problem Management Plus (PM+) program delivered by trained counselors.

5 sessions (in-person)

Booster Session

Duration - 1 session lasting about 60 minutes

Approximately three months after completing PM+, participants randomized to the booster group receive a one-time PM+ booster session to refresh PM+ strategies and practice skills.

1 visit (in-person) for booster session

Follow-up Assessments

Duration - Up to 6 months after baseline

Participants complete follow-up assessments approximately one week after PM+, three months after PM+ (coinciding with booster or phone reminder), and six months after PM+ to evaluate outcomes.

3 assessment points via electronic surveys and qualitative interviews

Trial Site Locations

Total: 1 location

1

Grand Bahama Resilience Center

Freeport, Grand Bahama, The Bahamas

Actively Recruiting

Loading map...

Research Team

C

Caroline McEneaney L McEneaney, JD, MA

A

Adam Brown D Brown, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Similar Trials

Effects of Baduanjin Breathing Training for Depression and A...

Depression Symptoms

Actively Recruiting

1 location

Culturally and Language-Adapted i-CBT for Common Mental Heal...

Depressive Symptoms

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial

Effect of a Multicomponent Behavioral Intervention in Adults Impaired by Psychological Distress in a Conflict-Affected Area of Pakistan: A Randomized Clinical Trial.

Atif Rahman, Syed Usman Hamdani, Naila Riaz Awan...

https://pubmed.ncbi.nlm.nih.gov/27837602

Problem Management Plus (PM+): a WHO transdiagnostic psychological intervention for common mental health problems.

Katie S Dawson, Richard A Bryant, Melissa Harper...

https://pubmed.ncbi.nlm.nih.gov/26407793

Effectiveness of a brief behavioural intervention on psychological distress among women with a history of gender-based violence in urban Kenya: A randomised clinical trial.

Richard A Bryant, Alison Schafer, Katie S Dawson...

https://pubmed.ncbi.nlm.nih.gov/28809935