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Completed

NCT Number: NCT00979784

Better Weight-Better Sleep (BWBS) Trial

The hypothesis of this study is that overweight and obese patients exposed to sleep focused counseling and standard dietary and exercise counseling will have better outcomes than similar patients exposed to standard dietary and exercise counseling only.

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Key information

Age range

18 year–84 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Family Medicine Center, Summa Health System

Akron, Ohio, 44309, United States

About this study

Objective: To explore the feasibility of integrating sleep management interventions with dietary and exercise interventions for obesity in a 12-week randomized trial. Methods: We randomized 49 overweight or obese adult patients either to a better weight (BW) cognitive behavioral intervention, or to a combination of the BW intervention and a better sleep intervention, better weight-better sleep (BWBS). Results: The BWBS group lost weight faster (P=.04), and coping self-efficacy accelerated (P=.01). Conclusions: These preliminary results merit replication in a larger primary care-based trial with a longer continuous intervention and followup period. Key words: obesity, sleep, weight loss, primary care, health behavior E Logue et al. Am J Health Behav. 2012;36(3):319-334 DOI: http://dx.doi.org/10.5993/AJHB.36.3.4

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • BMI 25 to 39.9
  • ages 18 to 84
  • PCP permission
  • patient in Family Medicine Center with an encounter in the last six months

Exclusion criteria

  • various obesity and sleep related disorders

Treatment and study plan

Better Weight

Behavioral

Standard cognitive behavioral treatment focused on dietary & exercise behavior

Better Weight & Better Sleep

Behavioral

Standard CBT to support dietary and exercise change plus sleep hygiene and sleep focused CBT

Primary outcomes

  1. percent baseline weight lost

    Time frame: 16 weeks

Secondary outcomes

  1. feasibility, variance-covariance estimates

    Time frame: 16 weeks

Sponsors and collaborators

Lead sponsor

Summa Health System

Other

Collaborators

  • Northeastern Ohio Universities College of Medicine
  • Ross Products

Registry information

Official study title

The Better Weight-Better Sleep Study: A Pilot Intervention in Primary Care

Acronym: BWBS

Important dates

Study start
2009
Primary completion
2011
Study completion
2012
First posted
Sep 18, 2009
Registry last updated
Jun 12, 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.

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