Clinical trial for Cognition
Official title Dietary Supplements and Middle Aged Women (Creatine)
ClinicalTrials.gov ID: NCT07729930
What this study is testing
- What it's testing
- This study will examine the effects of combining different types of dietary supplements on various aspects of health and wellbeing in middle aged women. The main outcomes of the trial will be aspects of health and wellbeing that middle aged women report as increasingly problematic, such as joint pain, fatigue, sleep, and changes in body composition, strength, and inflammation.
- You might receive a placebo (an inactive treatment) instead of the study drug, decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 35 to 65, women only. Healthy volunteers may be eligible.
You may be able to join if
- Female
- Aged 35-65 years old
- Healthy, free from known disease
- Non-smoker
- BMI 18-30 kg/m2
You likely can't join if
- Currently have a musculoskeletal injury or diagnosed condition (CVD, osteoarthritis, diabetes, cancer, metabolic syndrome, uncontrolled hypertension...
- Regularly taking prescription medication initiated in the last 3 months or unstable
- Have initiated hormone replacement therapy within the last 3 months or unstable
- Have an allergy to ingredients in the supplements or standardised breakfast
- Pregnant or breastfeeding, or any other contradictions to consuming the study supplements
- Lost more than 10% of body mass in the past 6 months or plan on trying to lose body mass during trial period
See the full eligibility criteria
- Female
- Aged 35-65 years old
- Healthy, free from known disease
- Non-smoker
- BMI 18-30 kg/m2
- Classified as recreationally active (meet the WHO guidelines for physical activity: complete at least 150-300 minutes of moderate intensity activity or 75-150 minutes of vigorous intensity activity a week, plus muscle...
- Currently have a musculoskeletal injury or diagnosed condition (CVD, osteoarthritis, diabetes, cancer, metabolic syndrome, uncontrolled hypertension, gastrointestinal disease, blood clotting disorder)
- Regularly taking prescription medication initiated in the last 3 months or unstable
- Have initiated hormone replacement therapy within the last 3 months or unstable
- Have an allergy to ingredients in the supplements or standardised breakfast
- Pregnant or breastfeeding, or any other contradictions to consuming the study supplements
- Lost more than 10% of body mass in the past 6 months or plan on trying to lose body mass during trial period
- Currently consuming the supplements being investigated and unwilling to stop
- Any known cognitive or visual impairments limiting ability to perform cognitive tests
- Unwilling to maintain current diet and physical activity levels and report any change in health status
The study team makes the final eligibility decision.
Where it's taking place
- Loughborough, United Kingdom
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 35 years to 65 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Loughborough, United Kingdom. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.