Skip to main content
OpenTrials
Completed

NCT Number: NCT01203995

Remote Information Counseling for Elders

The purpose of this study is to provide testing methods of delivering nutrition and physical activity services for weight loss.

Completed

Looking for future studies?

Notify Me

Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

HITS

Indianapolis, Indiana, 46205, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 40 to 64 years.
  • One or more CHC visits in the past 12 months.
  • Body-mass index of ≥30 and <50.
  • English speaking.
  • Access to telephone.
  • A permanent address.
  • Willingness to be randomized.
  • Willingness to have computer installed in home.

Exclusion criteria

  • Any serious medical condition likely to hinder accurate weight measurement, or for which weight loss is contraindicated or could cause weight loss (e.g., cancer).
  • Current diagnosis of psychosis or bipolar disorder.
  • Unstable or recent onset of cardiovascular disease within 6 months or presence of congestive heart failure
  • Illness that might be associated with weight change, such as asthma (because of treatment with corticosteroids), psychosis
  • Use of medications that might cause weight gain such as hypoglycemic oral medicines or insulin, anti-depressants, and weight loss medications.
  • Unwilling or unable to provide informed consent.
  • Receiving disability insurance.
  • Pregnant or nursing in past 6 months, or plans to become pregnant within 12 months.
  • Enrolled in a weight loss program or study or member of household enrolled in study.
  • Residence outside of Marion County, Indiana.
  • Residence relocation plans within 12 months.
  • Planned or prior bariatric surgery.
  • Substance abuse.
  • History of treatment for eating disorder.
  • Unstable weight with loss or gain of ≥ 5% in last 3 months.

-

Treatment and study plan

Nutrition information

Behavioral

Brief nutrition education with take home reference materials and portion size tools

Nutrition education and exercise training

Behavioral

Twice per week nutrition education and exercise class held either in-clinic or through vide-conference.

Primary outcomes

  1. BMI

    Time frame: two months

Secondary outcomes

  1. 2-Minute Step Test

    Time frame: two months

    Number of steps completed in two minutes

  2. Chair stand test

    Time frame: 2 month

Sponsors and collaborators

Lead sponsor

Indiana University

Other

Registry information

Acronym: RICE

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Sep 17, 2010
Registry last updated
Apr 2, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.