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Dietary Interventions for Osteoarthritis Pain (DIRECTPain Trial)
N/A
Recruiting
Led By Robert E Sorge, PhD
Research Sponsored by University of Alabama at Birmingham
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline (week 0), immediately before the intervention (week 3), 3 weeks after initiating the intervention (week 6), immediately after the intervention (week 9)
Awards & highlights
No Placebo-Only Group
Summary
This trial will investigate the efficacy of low-carb diets to reduce knee OA pain, with an emphasis on racial differences and interactions with biopsychosocial factors. #OA #RacialDisparities #PainRelief #LCD
Who is the study for?
This trial is for English-speaking adults aged 40-75 with knee osteoarthritis, who self-identify as either Non-Hispanic Black or White, have a BMI of 25-40, eat more than 100g of carbs daily, and experience pain most days. Excluded are those on opioids or certain other meds, with recent weight change, major surgery like knee replacement, severe diseases affecting heart/lungs/digestion/metabolism, extreme exercisers or dieters.
What is being tested?
The study tests if a low-carbohydrate diet can reduce pain and improve quality of life in people with knee OA compared to the standard USDA diet. It will also look at how race might affect these outcomes by focusing on differences between Non-Hispanic Blacks and Whites.
What are the potential side effects?
While not explicitly stated in the provided information, potential side effects from dietary changes may include digestive discomforts such as constipation or diarrhea due to shifts in fiber intake; fatigue during initial adjustment periods; and possible nutrient deficiencies if not properly managed.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline (week 0), immediately before the intervention (week 3), 3 weeks after initiating the intervention (week 6), immediately after the intervention (week 9)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline (week 0), immediately before the intervention (week 3), 3 weeks after initiating the intervention (week 6), immediately after the intervention (week 9)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
BPI pain change
TUG pain intensity change
Western Ontario and McMaster Osteoarthritis Index pain change
Secondary study objectives
BPI pain interference change
PHQ-9 Depression change
Repeated Chair Stand pain intensity change
+3 moreOther study objectives
Repeated Chair Stand time to completion change
TBARS change
TUG time to completion change
+2 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Non-Hispanic WhiteExperimental Treatment2 Interventions
White adults ages 40-75 with knee OA.
Group II: Non-Hispanic BlackExperimental Treatment2 Interventions
Black adults ages 40-75 with knee OA.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Low-carbohydrate diet
2007
N/A
~160
USDA Diet
2018
N/A
~30
Find a Location
Who is running the clinical trial?
University of Alabama at BirminghamLead Sponsor
1,645 Previous Clinical Trials
2,342,652 Total Patients Enrolled
8 Trials studying Osteoarthritis
44,432 Patients Enrolled for Osteoarthritis
Robert E Sorge, PhDPrincipal InvestigatorUniversity of Alabama at Birmingham
1 Previous Clinical Trials
20 Total Patients Enrolled
1 Trials studying Osteoarthritis
20 Patients Enrolled for Osteoarthritis
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have lost or gained more than 4 kg in the last month.I have diabetes and am not taking medication for it.I have not been hospitalized for an eating or psychiatric disorder in the last 6 months.I am taking medication that affects my metabolism or digestion.I have experienced pain most days for the last 3 months.I have trouble chewing or swallowing.I have heart or lung disease.I have a digestive system condition.I have been diagnosed with knee osteoarthritis.I have had a knee replacement.I am between 40 and 75 years old.I rely on others to prepare my meals.I take opioid painkillers every day.I am taking blood pressure medication that affects my blood sugar levels.
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Research Study Groups:
This trial has the following groups:- Group 1: Non-Hispanic Black
- Group 2: Non-Hispanic White
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