MORPH-A: Multidisciplinary Obesity Rehabilitation & Psychophysical Health and Awareness
Official title: MORPH-A - Multidisciplinary Obesity Rehabilitation & Psychophysical Health and Awareness. A Multidisciplinary Outpatient Rehabilitation Programme for Obese Patients With Comorbidities
Run by Istituti Clinici Scientifici Maugeri SpA · NCT07880847 · Data updated 2026-11-12
This program tests a 12-week multidisciplinary obesity rehabilitation and care management plan for adults with class I–II obesity and related risks who are starting GLP-1 or GLP-1/GIP therapy.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 34 (estimated) |
| Sponsor | Istituti Clinici Scientifici Maugeri SpA Academic / other |
| Locations | 1 site (Pavia) |
| Status | Recruiting |
| Started | August 25, 2026 |
| Main results expected | May 31, 2028 |
| Study ends | November 30, 2028 |
| Registry record updated | October 19, 2026 |
| Trial ID | NCT07880847 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults over 18 with class I or II obesity (BMI 30–39.9) and cardiometabolic risk factors (EOSS ≥ 2) who are starting GLP-1 or GLP-1/GIP therapy and can participate in a 12-week outpatient program.
✕Probably not a fit
Patients without access to GLP-1 (or GLP-1/GIP) therapy or those unable to participate in physical activity may see limited benefit from this program.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This intervention combines multidisciplinary rehabilitation with routine clinical management to support adults with obesity and cardiometabolic risk factors. Eligible participants start GLP-1 or GLP-1/GIP therapy and engage in a 12-week program designed to address physical activity, nutrition, and psychosocial factors. The study emphasizes outpatient care, structured exercise, and ongoing care coordination within an Italian clinical setting. Participant suitability includes language comprehension, stability for physical activity, and informed consent. Outcomes focus on feasibility, adherence, and potential improvements in health risk profiles.
Why it matters
Potential benefit: If successful, participants may experience improvements in weight-related health risks and quality of life through integrated medical and rehabilitative care.
How similar studies have gone: Multidisciplinary obesity rehabilitation approaches have shown promise in improving weight management and metabolic risk factors in similar outpatient settings.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age \>18 years * Class I or II obesity assessed at T0 with comorbid risk factors (EOSS \> or equal to 2) for which an SIO appropriateness form with a score \> or equal to 20 has been completed * Patients who agree to begin treatment with a GLP-1 or GLP-1/GIP analog * Fit for physical exercise * Willingness to participate in the 12-week program * Understanding of the Italian language and ability to complete the questionnaires * Understanding of the research objectives and ability to provide informed consent. Exclusion Criteria: * Age \< 18 years; * Non-Italian education, illiteracy, or relapse into illiteracy; * Low motivation/interest or refusal to undergo assessment; * Absence of comorbidities (EOSS \< or equal to 1) * Major psychiatric disorders, substance abuse; * Obesity secondary to genetic and endocrinological disorders (e.g., hypercortisolism, acromegaly, overt hypothyroidism); * Functional limitations that prevent participation in physical therapy sessions; * Concurrent participation in other trials that could potentially interfere with the outcomes of this study.
Where it's running
-
Istituti Clinici Scientifici Maugeri, IRCCS
Pavia, Italy Recruiting
Study contacts
- Principal investigator: Antonia Pierobon — Istituti Clinici Scientifici Maugeri IRCCS
- Study coordinator: Antonia Pierobon
- Email: antonia.pierobon@icsmaugeri.it
- Phone: +390385247255
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Ocular Changes in People Using Tirzepatide or Semaglutide
This study checks whether eye structure and blood vessels change in adults with obesity who are taking semaglutide or tirzepatide as part of routine care.
-
Whole-Body Vibration Training in Women With Obesity With and Without Type 2 Diabetes
This study tests whether eight weeks of supervised whole-body vibration training changes ankle muscle activity and walking performance in women with obesity, comparing those with and without type 2 diabetes.
-
Berobenatide for knee pain in adults who are overweight or with obesity
This study tests berobenatide vs. placebo to see if it reduces knee pain and improves function while helping with weight in adults with knee osteoarthritis and overweight/obesity.
-
Weekly berobenatide for knee osteoarthritis in adults who are overweight or obese
This study tests whether weekly berobenatide helps reduce knee pain and improve function, while also affecting body weight, in adults with knee osteoarthritis who are overweight or obese (with or without type 2 diabetes).
-
Maridebart cafraglutide in people who switched from weekly GLP-1 receptor agonists
This study tests how much maridebart cafraglutide appears in the blood after people with overweight or obesity switch from weekly GLP-1 receptor agonists.
-
EloraTZP for weight loss in adults with overweight/obesity and type 2 diabetes
This trial tests whether a coformulation of eloralintide and tirzepatide helps people with obesity or overweight and type 2 diabetes lose weight compared with tirzepatide alone.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.