Recruiting

Magnesium & Melatonin

Sponsor:

StudySetGo

Code:

NCT07651514

Conditions

Poor Sleep Quality

Leg Cramps, Nocturnal

Eligibility Criteria

Sex: All

Age: 40 - 70+

Healthy Volunteers: Accepted

Interventions

Magnesium and melatonin based multi-ingredient dietary supplementation

Placebo

Study Details

Brief summary:

Participants are being invited to take part in a research study. Before deciding whether to take part, it is important for participants to understand why the research is being done and what it will involve.

Purpose: This study will investigate whether a multi-ingredient nutritional supplement containing magnesium and melatonin can improve sleep quality in adults who experience disrupted sleep due to nighttime leg cramps.

What participation involves: Participation lasts 8 weeks. Participants will be randomly assigned to take either the nutritional supplement or a placebo (inactive look-alike) every night before bed for 6 weeks. Participants will wear an Oura Ring wearable device on one finger continuously for 8 weeks throughout the study and complete short questionnaires using a smartphone app. The Oura Ring and study supplement will be sent to the participant's home address. Participants will never need to travel to a research centre; all contact with the research team will be by video call, phone, messaging, or email.

How long: Total involvement will be 8 weeks, made up of a 2-week baseline period and a 6-week supplementation period. Each day, participants will complete a short app-based questionnaire (approximately 1 minute). At the end of weeks 2, 4, 6, and 8, participants will complete additional app-based questionnaires (approximately 10 minutes).

Conditions

Poor Sleep Quality

Leg Cramps, Nocturnal

Study ID

NCT07651514

Start date

Oct 10, 2026

Status verified date

Oct, 2026

Completion date

Sep 10, 2027

Anticipated

Primary completion date

Sep 10, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 40 - 70+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • Adults aged 40-75 years
  • Self-reported poor sleep quality (PSQI >5) at screening
  • Self-reported nocturnal leg cramp averaging ≥4 episodes per fortnight at screening
  • Capacity to understand and provide electronic informed consent
  • Willing to wear an Oura Ring wearable device continuously throughout the study period
  • Access to a smartphone/tablet with iOS 15 or higher and Android 9 or higher and willing to install and use the Oura and Trialflare applications
  • Be a resident of and permanently living in Florida with no planned travel across more than one time zone for at least 1 night during the study period

Exclusion Criteria:

  • Current or recent (within 4 weeks of randomisation) use of melatonin, magnesium, or other supplements specifically taken for sleep or leg cramps or listed as an ingredient of the intervention supplement.
  • Current use of any prescription medication
  • Diagnosed sleep disorder (e.g. obstructive sleep apnoea, restless legs syndrome, insomnia disorder)
  • Known or suspected secondary cause of nocturnal leg cramps (e.g. peripheral vascular disease, neurological condition, renal impairment, thyroid disorder)
  • Any current or prior diagnosis of:
  • Cancer or malignancy of any kind (prior malignancy is not exclusionary if the participant is in confirmed remission and has completed all treatment)
  • Cardiovascular disease (e.g. hypertension, coronary artery disease, heart failure, arrhythmia, stroke, peripheral vascular disease)
  • Autoimmune disorder (e.g. rheumatoid arthritis, lupus, multiple sclerosis)
  • Gastrointestinal disorder (e.g. IBS, malabsorption syndromes)
  • Neurological disorder (e.g. epilepsy, Parkinson's disease, dementia)
  • Hepatic or renal impairment
  • Diabetes mellitus (type 1 or type 2)
  • Severe psychiatric disorder (e.g. schizophrenia, bipolar disorder)
  • Myasthenia Gravis
  • Known hypersensitivity or allergy to any ingredient in the active or placebo product
  • Rotating shift work or irregular sleep patterns
  • Current participation in another interventional clinical trial
  • Inability to comply with study procedures or remote visit schedule
  • Breastfeeding, pregnant, or planning to become pregnant during the study period

Study Design

Enrollment

50 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Magnesium and melatonin based multi-ingredient dietary supplement

placebo comparator: Placebo

Interventions

Magnesium and melatonin based multi-ingredient dietary supplementation

The active intervention is a commercially available multi-ingredient dietary supplement, supplied by Imagine Biolabs LLC (trading as SaltWrap) and sold under the brand name Mag R\&R. The dose is up to 3 capsules per day taken 30 minutes before bedtime with water. The product is stored at room temperature.

Placebo

The placebo is manufactured by the same manufacturer that produces the active product (Vitaquest International, New Jersey, USA). The placebo is visually similar to the active product and will be packaged in the same plain bottles as the active intervention to maintain the blind. The placebo dose is up to 3 capsules per day taken with water. Packaging is managed by Vitaquest International.

Primary outcome measure

  • Pittsburgh Sleep Quality Index (PSQI) [ Time Frame: From enrollment to the end of treatment at 6 weeks ]

Central Contacts and Locations

Central contacts

Christopher Koscien, PhD

+447847617414misit@studysetgo.com

Tom Jameson, PhD

+447794865520tom.jameson@studysetgo.com

Locations

StudySetGo Decentralised team

Recruiting

Palm Beach Gardens, Florida, United States, 33418

Contacts

Tom Jameson

+44 7794865520tom.jameson@studysetgo.com

More Information

Sponsor

StudySetGo

Last update posted

Oct 14, 2026

Last verified

Oct, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-24. This information was provided to ClinicalTrials.gov by StudySetGo on 2026-10-14. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.