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OpenTrials
Completed

NCT Number: NCT01211574

Pilot Study Testing Professional, Peer, and Mentor Health Coaches for Weight Loss

Participants will be randomly assigned to 1 of 3 types of health coaches, Peers, Mentors, or Professionals. The aim of this study is to examine the feasibility and preliminary efficacy of health coaching for weight loss.

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Key information

Age range

40 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • age 40-60

Exclusion criteria

  • Participants will be excluded if they:
  • Are unwilling to participate in a weight control program that includes weight coaches.
  • Report not being able to walk 2 blocks (1/4 mile) without stopping.
  • Are participating in a weight loss program, taking a weight loss medication, have a history of bariatric surgery, or lost ≥ 5% of body weight during the past 6-months.
  • Are pregnant, lactating, less than 6 months post-partum or plan to become pregnant during the time of the intervention.
  • Report a heart condition, chest pain during periods of rest or activity, or loss of consciousness on the Physical Activity Readiness Questionnaire (PAR-Q). Participants reporting joint problems, medication use, or other medical conditions that may limit their ability to exercise will be required to obtain written permission from their physician to participate in the intervention.
  • Report conditions that, in the judgment of the PI, would render the participant unlikely to follow the study protocol (e.g., terminal illness, relocation, substance abuse, bulimia nervosa, dementia, or severe psychiatric condition).

Treatment and study plan

Peer Coach

Behavioral

Participants will receive behavioral weight loss treatment and be coached by a peer between treatment visits.

Mentor

Behavioral

Participants will receive behavioral weight loss treatment and be coached by a mentor between treatment visits.

Professional

Behavioral

Participants will receive behavioral weight loss treatment and be coached by a behavioral weight loss interventionist between treatment visits.

Primary outcomes

  1. weight change

    Time frame: 0 to 6 months

Sponsors and collaborators

Lead sponsor

The Miriam Hospital

Other

Registry information

Important dates

Study start
2010
Primary completion
2011
Study completion
2011
First posted
Sep 29, 2010
Registry last updated
Jul 13, 2012

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.

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