The Impact of Probiotic Supplementation on the Well-being of Women.
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Female
- Sponsor
- Cultech Ltd
- Enrollment
- 50
- Locations
- 1
- Primary Endpoint
- Mood Questionnaire
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
An exploratory study to determine whether daily supplementation with a probiotic product impacts the overall well-being of women aged between 45 - 65
Detailed Description
It is generally accepted that there is a gradual decline in general well-being associated with aging. In previous studies with healthy adults receiving the Lab4P probiotic the outcomes indicated an overall improvement in general well-being and these findings provide the focus for the current trial which is investigating whether daily supplementation with the Lab4P probiotic product can impact upon the well-being of a cohort of women aged between 45 - 65 years (peri-menopausal/menopausal/post-menopausal). The trial will be a double blinded, 2-arm, randomized, placebo-controlled, parallel group superiority study consisting of 50 women (gender as assigned at birth), aged between 45-65. The randomisation scheme will be generated by using a web-based interface using 1:1 allocation into 2 groups (block size 2). The participants will make two site visits, the first visit for enrolment when they will be randomised, allocated their appropriate study product and their height, body weight and blood pressure will be measured. They will also be given a series of questionnaires assessing sleep (Athen Insomnia Scale), Mood (Hospital Anxiety and Depression Scale) and Quality of Life (Menopause Rating Scale) together with two cognitive tests (Word colour Stroop and Rey Auditory Verbal Learning Test (RAVLT)) to complete. A blood sample, a stool sample and a vaginal swab will be collected at this visit (if possible) and the participant will be given sample collection kits to take with them to collect futher samples prior to their second visit. They will be given a copy of each of the questionnaires and requested to be completed them and return by post at the study midpoint (day 56). They will also receive a copy of a Well-being diary that they will be asked to complete weekly throughout the study. The second visit will take place at the end of the study (around day 112) and at that time the participants will bring the stool sample and vaginal swab collected at home and provide the final blood sample. At this time the participants will also complete each of the questionnaires (sleep, mood and quality of life) on site and repeat the Word Colour Stroop and RAVLT tests. The completed weekly Well-being diaries and any unused intervention will be returned. Scientists will use the information and samples collected to assess the benefits of taking the probiotic supplement. It is considered that the daily intake of the probiotics will improve general wellbeing and mental health. Due to the chance that the use of the placebo, it is possible that any benefits will be confined to the participants who are randomly assigned the probiotic product. It is envisaged that the results generated from this study will enhance and improve our understanding of the benefits of daily probiotic supplementation. There is no record of any adverse reactions associated with the regular consumption of this probiotic product but participants may experience mild side effects such as a change in bowel habit and/ or increased flatulence (intestinal gas) during the first few days of taking the supplement.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Women aged 45 to 65
- •Willing to provide faecal samples, blood samples and vaginal swabs
- •BMI of less than 30 kg/m2
- •Willing to maintain normal diet and lifestyle during the study
- •Willing to refrain from taking other probiotic supplements during the study
- •Normal (or corrected-to-normal) vision without colour blindness in order to complete the cognitive task
Exclusion Criteria
- •No oral antibiotics within the last 3 months
- •No previous been involvement in a Cultech funded study
- •No regular consumption of probiotics within the last 1 month prior to the study
- •Premature menopause (onset before age of 40)
- •Given birth in the last 3 months, currently pregnant or planning pregnancy
- •Receiving hormone replacement therapy
- •Shift worker
- •Diagnosed with diabetes
- •Immunodeficient or undergoing immunosuppressive therapy
- •Diagnosed with arrhythmia, ventricular extrasystole or atrioventricular block
Outcomes
Primary Outcomes
Mood Questionnaire
Time Frame: At Day 1, Day 56 and Day 112 ± 3 after trial start
Mood questionnaires to evaluate the participants mood post probiotic supplementation. This mood questionnaire is based off the Hospital Anxiety Depression Scale (HADS) and uses a four point scale for severity ranging from "0 - 3" with 0 being the lowest symptom severity and 3 being the highest symptom severity.
Sleep Quality Questionnaire
Time Frame: At Day 1, Day 56 and Day 112 ± 3 after trial start
Sleep quality questionnaire to measure the participants quality of sleep post probiotic supplementation. This sleep questionnaire uses the Athens Insomnia Scale and reports sleep quality using select phrases, and not a scored scale, such as "no problem, minor problem, considerable problems, serious problems". These phrases are question dependent.
Quality of Life Questionnaire
Time Frame: At Day 1, Day 56 and Day 112 ± 3 after trial start
Quality of life questionnaire to evaluate the participants quality of life post probiotic supplementation. This QoL questionnaire uses a non-numeric, 5-point scale, ranking the presence and severity of symptoms as "none, mild, moderate, severe, and extremely severe".
Secondary Outcomes
- Bacterial composition of faecal samples via sequencing(At Day 1 and Day 112 ± 3 after trial start)
- Weekly Well-being Diary(Days 1, 7, 14, 21, 28, 35, 42, 49, 56, 63, 70, 77, 84, 91, 98, 105 and 112)
- Bacterial composition of vaginal samples via sequencing(At Day 1 and Day 112 ± 3 after trial start)
- Blood plasma analysis for plasma lipids(At Day 1 and Day 112 ± 3 after trial start)
- Blood plasma analysis inflammatory markers(At Day 1 and Day 112 ± 3 after trial start)