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NCT Number: NCT07446907

Optimizing Adaptive Intensive Behavioral Therapy for Obesity During the Transition to Older Adulthood

To test adaptive intensive behavioral therapy strategies comprising dietary patterns with varying amounts of protein and including supplemental protein or resistance exercise training for promoting weight loss and attenuating lean mass loss in adults aged 50-75 with obesity.

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Key information

Age range

50 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Alabama at Birmingham

Birmingham, Alabama, 35233, United States

Location contact

Drew Sayer, MD

PRINCIPAL_INVESTIGATOR

About this study

This Sequential Multiple Assignment Randomized Trial (SMART) seeks to identify the optimal initial dietary strategy (high vs. standard protein diets) and as-needed augmentation strategy (protein supplementation vs. supervised resistance exercise training) for behavioral weight loss in adults aged 50-75. Augmentation strategies will only be used for participants who do not achieve at least 3% weight loss and/or those who lose more than 1.5 kg of fat free mass (i.e., Non-Responders) after 8 weeks of group-based behavioral obesity treatment. Protein supplements and supervised resistance exercise training will be provided at no-cost to participants for weeks 9-16 of the study. Responders (i.e., achieving at least 3% weight loss and less than 1.5 kg loss of fat free mass) will continue with their initial high protein or standard protein diet assignment for the remainder of the trial. This SMART will enroll 250 adults aged 50-75 years with a BMI of at least 30 kg/m2. All participants will receive 1 year of behavioral obesity treatment including 16 weeks of weekly group-based treatment (active weight loss phase) followed by 36 weeks of monthly group sessions to promote continued engagement in dietary and exercise behaviors and long-term weight loss maintenance. The behavioral intervention will be delivered via Zoom. Data collection will occur at the University of Alabama at Birmingham and 5 study visits will be scheduled including: screening (to determine eligibility), prior to starting the weight loss intervention (baseline), and at weeks 8, 16, and 52.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Male or female sex
  • all racial and ethnic groups
  • BMI: 30-50 kg/m2
  • age 50-75 years
  • postmenopausal status for ≥1 y if female sex

Exclusion criteria

  • <3 months stable use of other medications affecting body weight or appetite
  • >450 pounds (due to weight limitations of the DXA)
  • indication or previous diagnosis of sarcopenia
  • existing kidney disease
  • current binge eating disorder, anorexia, or bulimia
  • untreated hyper- or hypothyroidism, cancer (except basal cell), gastrointestinal disorders affecting food intake or nutrient absorption; any other medical condition, as determined by the study physician, precluding a HP diet and/or daily exercise

Treatment and study plan

High Protein Diet Counceling

Behavioral

16 week group-based weight loss program with counseling to consume a high protein diet. Approximate macronutrient distributions (carbohydrate:protein:fat) will be 32%:40%:28%.

Standard Protein Diet Counceling

Behavioral

16 week group-based weight loss program with counseling to consume a standard protein diet. Approximate macronutrient distributions (carbohydrate:protein:fat) will be 53%:20%:27%.

Protein Supplement

Behavioral

Non-responders from either initial randomized group assigned to this intervention receive twice daily protein supplements.

Supervised exercise

Behavioral

Non-responders from either initial randomized group assigned to this intervention receive twice weekly small-group supervised resistance exercise training sessions.

Primary outcomes

  1. Change in Body Weight

    Time frame: Baseline, 8 weeks, 16 weeks, 52 weeks

    Participants will be weighed at baseline through 52 weeks

  2. Change in Fat Free Mass

    Time frame: Baseline, 8 weeks, 16 weeks, 52 weeks

    Participants will be scanned via DXA scan to measure overall fat free body mass

Secondary outcomes

  1. Change in Fat Mass

    Time frame: Baseline, 8 weeks, 16 weeks, 52 weeks

    Participants will be scanned via DXA scan to measure overall fat mass

  2. Change in Fasting Glucose

    Time frame: Baseline, 8 weeks, 16 weeks, 52 weeks

    Participants will have a blood draw to check fasting blood sugar levels

  3. Change in Fasting Insulin

    Time frame: Baseline, 8 weeks, 16 weeks, 52 weeks

    Participants will have a blood draw to check fasting insulin levels

  4. Change in Fasting Hemoglobin A1C

    Time frame: Baseline, 8 weeks, 16 weeks, 52 weeks

    Participants will have a blood draw to check fasting A1C levels

  5. Change in Fasting LDL-cholesterol

    Time frame: Baseline, 8 weeks, 16 weeks, 52 weeks

    Participants will have a blood draw to check fasting LDL-cholesterol levels

  6. Change in Fasting HDL-cholesterol

    Time frame: Baseline, 8 weeks, 16 weeks, 52 weeks

    Participants will have a blood draw to check fasting HDL-cholesterol levels

  7. Change in Fasting Total Cholesterol

    Time frame: Baseline, 8 weeks, 16 weeks, 52 weeks

    Participants will have a blood draw to check fasting total cholesterol levels

  8. Change in Fasting Total Triglycerides

    Time frame: Baseline, 8 weeks, 16 weeks, 52 weeks

    Participants will have a blood draw to check fasting triglyceride levels

  9. Change in Blood Pressure

    Time frame: Baseline, 8 weeks, 16 weeks, 52 weeks

    Participants will have a blood pressure check at each appointment

  10. Change in Hand Grip Strength

    Time frame: Baseline, 8 weeks, 16 weeks, 52 weeks

    Participants will have hand grip strength via the Jamar dynamometer, a tool for assessing and monitoring patients' hand strength. Measurements are based on a scale of 0-90 kilograms of force, where higher numbers indicate more strength.

  11. Change in Lower Extremity Strength

    Time frame: Baseline, 8 weeks, 16 weeks, 52 weeks

    Participants will be assessed using the Short Physical Performance Battery (SPPB). The SPPB is a commonly-used assessment of lower extremity function in aging adults and used a combined score comprising tests of balance, gait speed, and the chair stand test.

    Key Components and Scoring (0-12 points total):

    Standing Balance: Evaluates three stances (side-by-side, semi-tandem, tandem) held for 10 seconds each, scored up to 4 points.

    Gait Speed: Measures the time taken to walk 3 or 4 meters at a normal pace, scored up to 4 points.

    Chair Stands: Measures the time taken to rise from a chair five times without using arms, scored up to 4 points.

    Interpretation and Cut-off Scores:

    Total Score 0-6: Indicates low performance and high risk for functional decline.

    Total Score 7-9: Moderate performance. Total Score 10-12: High performance.

Sponsors and collaborators

Lead sponsor

University of Alabama at Birmingham

Other

Registry information

Official study title

Optimizing Adaptive Intensive Behavioral Therapy for Obesity During the Transition to Older Adulthood: A Sequential Multiple Assignment Randomized Trial

Important dates

Study start
2026
Primary completion
2031
Study completion
2031
First posted
Mar 3, 2026
Registry last updated
Apr 29, 2026

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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