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Weight Management & Wellness for People With Psychiatric Disabilities

University of Illinois logo

University of Illinois

Status

Completed

Conditions

Mental Illness
Obesity

Treatments

Behavioral: NEW-R

Study type

Interventional

Funder types

Other

Identifiers

NCT05128045
2016-0118

Details and patient eligibility

About

The purpose of this study is to conduct a randomized controlled trial to test the effectiveness of an intervention called Nutrition and Exercise for Wellness and Recovery (NEW-R) in promoting healthy eating and increased physical activity for better weight management among psychiatric outpatients.

Full description

Weight management is a serious issue for individuals with mental health conditions, especially those who are taking psychiatric medications. The latest estimates are that over half of individuals receiving community mental health services are overweight or obese. This project's objective is to conduct a randomized controlled trial to test the effectiveness of an intervention called Nutrition and Exercise for Wellness and Recovery (NEW-R) in promoting healthy eating and increased physical activity for better weight management among psychiatric outpatients living and working in the community. It is an 8-week, recovery-oriented intervention that is co-led by a trained health educator and a certified mental health peer specialist. The study will take place at the UIC Department of Psychiatry in Chicago. Research participants will be recruited from the Department's outpatient clinics and other community programs, and randomly assigned to receive NEW-R along with services as usual or services as usual alone.

Enrollment

113 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Diagnosis with a mental health disorder
  • Patient of outpatient program
  • Age 18 or older
  • Being overweight or obese defined as BMI>=25
  • Ability to understand spoken English

Exclusion criteria

  • Residing in a nursing home
  • Cardiac event in past 6 months
  • Past episode of anorexia or bulimia
  • Pregnancy
  • Diagnosis with a terminal illness expected to result in death within 1 year
  • Active alcohol or substance abuse or dependence
  • Inability to provide informed consent due to diagnosis of dementia or cognitive impairment
  • Inability to understand spoken English

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

113 participants in 2 patient groups

Experimental: NEW-R Intervention
Experimental group
Description:
NEW-R Intervention plus services as usual
Treatment:
Behavioral: NEW-R
Control
No Intervention group
Description:
Services as usual

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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