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4-week Seaweed Supplementation on Menopause Symptoms and Psychological Wellbeing

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Northumbria University

Status

Completed

Conditions

Menopausal Syndrome
Menopausal Depression

Treatments

Dietary Supplement: 500mg seaweed
Other: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT05759936
Project ID 2434

Details and patient eligibility

About

Menopausal symptoms have a substantial effect on quality of life as well as potentially serving as markers for future health. Previous research has suggested that diet can impact menopausal symptoms. Seaweed is marketed as a treatment to alleviate menopause symptoms, but no research has tested whether it is effective in reducing the symptoms and psychological effects associated with menopause.

The aim of this study is to investigate the effects of consuming a seaweed supplement over a 4-week time period on menopausal symptoms and psychological well-being.

Full description

Menopause and peri-menopause are associated with a number of symptoms and psychological well-being. Previous literature has found a relationship between diet and menopause management. For example, following the Mediterranean diet consuming a variety of vegetables, fruits, legumes and whole grains has found to improve menopausal symptoms particularly vasomotor symptoms. Few studies have explored the effects of dietary supplements on psychological well-being in menopause. The aim of the study is to explore the impact of an iodine-rich seaweed food supplement on menopause symptoms and mental well-being in those experiencing menopause. Online assessments of symptoms will take place pre-intervention and post-intervention and will be compared to the effects of a placebo.

Enrollment

75 patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Self-assess as healthy
  • Experienced menopausal or peri-menopausal symptoms in the past 6 months

Exclusion criteria

  • Are currently taking HRT, anti-depressants, or anti-anxiety medication
  • Are lactating or pregnant (or seeking to become pregnant)
  • Have a thyroid disorder
  • Are currently taking iodine supplements
  • Have any relevant food intolerances

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

75 participants in 2 patient groups, including a placebo group

Placebo
Placebo Comparator group
Description:
Placebo capsule consumed for 28 days
Treatment:
Other: Placebo
500mg seaweed
Experimental group
Description:
Seaweed capsule consumed for 28 days
Treatment:
Dietary Supplement: 500mg seaweed

Trial contacts and locations

1

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Central trial contact

Michael Smith; Crystal Haskell-Ramsay

Data sourced from clinicaltrials.gov

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