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RecruitingNCT07213466

Individualized Pharmacological Approach to Obesity in Patients With Bipolarity

This study is recruiting. It focuses on bipolarity and currently lists participation information in the United States.

BipolarityBehavioralFrom 18 Years to 65 Years
In plain English

Key information made simple

This study is looking at whether a digital support tool can help people with bipolarity. Participants receive a study treatment and complete follow-up visits and assessments. Taking part may give some people access to a digital support tool, but direct benefit is not guaranteed.

What to expect

Your next step

The official record suggests a mix of remote and in-person participation through a lab, with sites including Mayo Clinic in Rochester. Participation appears to involve questionnaires, interviews, or regular check-ins about day-to-day experience. The main fit is usually matching the main diagnosis and meeting the main study requirements, while common reasons not to take part include safety concerns that need urgent care first and active substance or alcohol problems that could affect the results. This is a later-stage study, which usually means the approach is being followed in broader real-world use.

Public study data

Key study information

Official title
Individualized Pharmacological Approach to Obesity in Patients With Bipolar Disorder - OBOE-Mayo
Condition
Bipolar I Disorder; Bipolar II Disorder; Schizo Affective Disorder; Obesity; Weight Loss; GLP - 1
Study status
Recruiting
Phase
Phase 4
Sponsor / lead affiliation
Mayo Clinic
Intervention
Group Therapy Program, semaglutide, Phentermine-Topiramate, naltrexone and bupropion (combination)
Location / country
United States
Contact
Laura N Harper, Karin M Lindstrom, Ph.D., Mark A Frye, M.D.
Email
harper.laura1@mayo.edu, lindstrom.karin@mayo.edu
Phone
507-255-9352, 507-293-3876
Registry
ClinicalTrials.gov
Why this study may matter

Why this study may matter

This study may matter because it is evaluating Group Therapy Program, semaglutide, Phentermine-Topiramate, naltrexone and bupropion (combination) in a structured research setting. For people exploring bipolarity research, clear information about the goal, status, contacts, and official source can support better questions before any decision.

Before joining

Questions to ask before joining

Official source

Registry reference

This page links back to the public source record so people can verify details directly with the registry and research team.

If you want the full study description, eligibility criteria, locations, and sponsor information in the original format, this is the place to check before taking the next step.

Open source record
Need help deciding?

Ask HopeStage to review this study with me

This form records your interest so HopeStage can follow up with practical guidance. It is not a medical eligibility decision and it does not guarantee a study spot.

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Study reference: NCT07213466. We only ask for your email here. HopeStage can help you review the study, but this is not a medical eligibility decision.
In practice

For you

Taking part may help test a support approach in real life.

It requires regular visits and structured follow-up.

Mixes in-person and remote participation.

Important

Not medical advice

Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com

Study clarity

Things to check before joining

Sponsor
Mayo Clinic
Sponsor type
Hospital / academic medical center
Main activity
digital app or tool
Intervention
Group Therapy Program, semaglutide, Phentermine-Topiramate, naltrexone and bupropion (combination)
Time commitment
long follow-up or multiple visits
Study phase
Phase 4
Enrollment
Not available
Recruitment status
Recruiting
Source
Official registry link
FAQ

Questions about this study

What is Individualized Pharmacological Approach to Obesity in Patients With Bipolarity?

This study is exploring digital app or tool for people with bipolarity. Participants may complete study visits, assessments, or follow-up activities defined by the research team. Direct benefit is not guaranteed.

Who is behind this study, and what type of sponsor is it?

This study is sponsored by Mayo Clinic. Based on the sponsor name or official registry information, it appears to be a hospital or academic medical center. You should verify the details in the official registry record.

What does participation involve, what phase is it, and what should I ask about safety?

This study may involve digital app or tool, study visits, and assessments. The time commitment is long follow-up or multiple visits. The study phase is Phase 4. Earlier-phase studies are often more focused on safety, dose, or feasibility, while later-phase studies usually involve more participants and more information about the intervention. The official source record gives the most accurate details. Enrollment is not available in HopeStage data. HopeStage cannot say whether a study is safe or right for you. Before joining, ask the research team about possible risks, time commitment, visits, side effects, compensation, safety monitoring, and whether participation may affect your current care.

Where can I verify the study details?

Use the official source record linked on this page to check the full study description, recruitment status, eligibility criteria, locations, sponsor information, phase, enrollment, contact details, and any listed risks or requirements.