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Internet Obesity Treatment Enhanced With Motivational Interviewing (iReach2)

University of Vermont logo

University of Vermont

Status

Completed

Conditions

Obesity

Treatments

Behavioral: Contingent MI
Behavioral: Internet Obesity Treatment
Behavioral: Internet Obesity Treatment with MI

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Internet-based weight control programs have been shown effective in producing weight loss, but in-person delivery of behavioral weight control produces significantly greater weight loss than on-line delivery of the same program. Motivational Interviewing has been shown to increase weight loss when delivered as an adjunct to in-person weight loss programs but has not been examined in conjunction with web-based obesity treatment. Therefore, the overall goal of this project is to determine if the addition of on-line Motivational Interviewing to a web-based group behavioral obesity treatment program will augment weight loss outcomes.

Full description

This randomized controlled trial is designed to determine whether weight losses in a group behavioral weight loss intervention conducted over the Internet are increased with the inclusion of individual, online MI sessions. All participants will receive the same online 6-month group-based behavioral weight loss program followed by 12 months of weight maintenance. Overweight and obese adults at two study sties (N=426) will be randomized to (1) Internet intervention; or 2) Internet intervention with individual MI sessions occurring at three month intervals on a fixed schedule (Internet+MI-Fixed). Assessments will be conducted every six months and will include measures of body weight and height, diet and exercise behaviors, Quality of Life, adherence measures (eg., attendance, compliance with self-monitoring), social influence components, motivation, treatment satisfaction, demographic data and descriptive information regarding use of website components. A third arm was added for the final 3 intervention cohorts. All participants received the program as described above with the addition of motivational interviewing contingent on participants' attendance in classes.

Enrollment

495 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • must be over 18
  • must have a BMI between 18 and 50
  • must live within 60 minutes driving distance of University of Arkansas, Little Rock, AR, or University of Vermont, Burlington, Vermont
  • must be able to walk for exercise

Exclusion Criteria:

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

495 participants in 3 patient groups

Internet Obesity Treatment
Active Comparator group
Description:
Participants will attend weekly class sessions on line and track food and exercise in an on-line journal.
Treatment:
Behavioral: Internet Obesity Treatment
Internet Obesity Treatment with MI
Experimental group
Description:
Participants will attend weekly classes on line, record food and exercise in an on-line journal, and will have no more than 6 individual motivational interviewing sessions.
Treatment:
Behavioral: Internet Obesity Treatment with MI
Contingent MI
Experimental group
Description:
Intervention is the same as for the MI arm, however participants will only receive MI if meeting certain treatment participation conditions.
Treatment:
Behavioral: Contingent MI

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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