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Delayed Onset Muscle SorenessPERFICTNCT07873866

Mineral-Infused Clothing for Recovery From Muscle Soreness and Muscle Damage After Exercise

A study testing Mineral-infused garment and Muscle-damaging eccentric exercise (drop jumps) in people with Delayed Onset Muscle Soreness and Exercise-Induced Muscle Damage, run by StudySetGo at 1 site in United Kingdom.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

The goal of this clinical trial is to learn whether wearing mineral-infused clothing helps muscles recover after a hard bout of unaccustomed exercise in healthy adults aged 18 to 45 who have not done lower-body resistance or jump training in the last 6 months. Read more about this study

Who is it for?
Ages 18 to 45 yearsHealthy volunteers can take part
What is being tested?
Mineral-infused garment and Muscle-damaging eccentric exercise (drop jumps)
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
52 participants
Where
1 siteUnited Kingdom
Study dates
Nov 2026to Apr 2027
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Adults aged 18 to 45 years inclusive
  • Body mass index between 18.5 and 29.9 kg/m2 inclusive
  • No participation in structured lower-limb resistance training or plyometric (jump) training within the previous 6 months (structured training: a planned programme of exercise against external load or bodyweight loading targeting the lower limbs, performed at least once per week for 4 or more consecutive weeks)
  • No history of injury that may impair the ability to perform maximal exercise
  • Willing to wear the allocated study garment for a minimum of 16 hours per day (approximately 8 hours waking and 8 hours overnight) throughout the 72-hour post-exercise recovery period, and during the muscle-damaging exercise protocol
  • Willing to maintain habitual diet and physical activity, including usual caffeine intake; to have the last meal and any caffeine at least 2 hours before each testing session; and to abstain from alcohol throughout the trial
Show all 10Show fewer
  • Able to attend the study site on four consecutive days
  • Able to provide written informed consent
  • Able to read, understand and communicate in English
  • Currently living in the United Kingdom

Who cannot join

  • Current use of non-steroidal anti-inflammatory drugs, corticosteroids or other anti-inflammatory medication
  • Current use of statins
  • Use of dietary supplements with known anti-inflammatory or antioxidant activity
  • Diagnosed muscle, neuromuscular or connective tissue disorders
  • Bleeding disorders or current use of anticoagulant medication
  • Known allergy or sensitivity to any material used in the study garment, or a history of textile or contact dermatitis
Show all 11Show fewer
  • Pregnancy, breastfeeding, or intention to become pregnant during the study period
  • Current participation, or participation within 4 weeks of screening, in another interventional clinical trial
  • Any condition that, in the opinion of the investigator, would compromise participant safety or data integrity
  • Current use, or use within 4 weeks, of any form of compression garment
  • Any response to the general health questions in the Screening Questionnaire indicating a contraindication to maximal exercise

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Christopher Koscien, PhD contact

+447847617414

perfict@studysetgo.com

United Kingdom1 site, 1 recruiting
  • StudySetGo

    Exeter

    Christopher Koscien, perfict@studysetgo.com

    Tom Jameson, PhD

    Recruiting

Other trials in United Kingdom

About this study

Official title: A Randomised, Double-Blind, Placebo-Controlled Trial to Evaluate the Effect of Mineral Infused Clothing on Recovery of Delayed Onset Muscle Soreness and Muscle Function Following Muscle Damaging Exercise

The goal of this clinical trial is to learn whether wearing mineral-infused clothing helps muscles recover after a hard bout of unaccustomed exercise in healthy adults aged 18 to 45 who have not done lower-body resistance or jump training in the last 6 months.

The main question it aims to answer is: does wearing the mineral-infused garment lead to greater recovery of leg muscle strength (maximal voluntary isometric contraction of the knee extensors) 72 hours after exercise, compared with wearing an identical garment without the mineral infusion?

Read more

Researchers will also compare the two garments for recovery of jump performance, muscle soreness and blood creatine kinase (a marker of muscle damage), and will describe garment comfort and tolerability.

Participants will:

  • Complete electronic consent, an online screening questionnaire and a video screening call
  • Attend the study site on four consecutive days
  • On Day 1, complete baseline tests, then perform 100 drop jumps (5 sets of 20) to cause muscle soreness
  • Wear their allocated garment for at least 16 hours a day (day and overnight) for the following 72 hours and keep a daily wear log
  • Have strength, jump and soreness tests and a finger-prick blood sample at each visit (24, 48 and 72 hours after exercise)
Read the detailed description

Unaccustomed exercise with a substantial eccentric component produces exercise-induced muscle damage, characterised by a transient loss of muscle force, delayed onset muscle soreness (DOMS) that typically peaks 48 to 72 hours after exercise, reduced explosive performance and a rise in circulating creatine kinase. Lower-limb garments are widely used to aid recovery, and meta-analyses of compression garments report small to moderate benefits for strength, power and perceived soreness. Mineral-infused textiles, marketed as re-emitting body heat as far-infrared radiation, form a poorly characterised category of recovery garment, and their effect on recovery from muscle-damaging exercise is unknown.

Design: single-site, randomised, double-blind, sham-controlled, parallel-group trial with 1:1 allocation, conducted at a StudySetGo study site in Exeter, United Kingdom. Randomisation uses computer-generated permuted blocks of varying size, stratified by sex. The control garment is manufactured to the same external specification, fabric, colour, sizing and finish as the active garment but without the mineral infusion, and is supplied in identical coded packaging.

Procedures: screening and consent are completed remotely (electronic consent and screening questionnaire via PandaDoc, followed by a Zoom screening call). On Day 1, participants are randomised and issued their garments, then complete baseline assessments in a fixed order: capillary blood sample, soreness visual analogue scale (100 mm, during a bodyweight squat), maximal voluntary isometric contraction (MVC) of the knee extensors of the dominant limb and squat jump. Participants then perform a muscle-damaging protocol of 100 drop jumps (5 sets of 20, 10 s between jumps, 2 min between sets) under one-to-one supervision, followed by 0-hour assessments. Garments are worn for a minimum of 16 hours per day (approximately 8 hours waking and 8 hours overnight) through the 72-hour recovery period, removed only for assessments and personal care, and wear is recorded in a daily log. Assessments are repeated at 24, 48 and 72 hours. Participants keep their habitual diet and caffeine intake, have their last meal and any caffeine at least 2 hours before testing, attend at the same time of day (plus or minus 1 hour) on each visit, and avoid alcohol, other recovery modalities, anti-inflammatory medication and strenuous exercise during the study. A Study Exit Questionnaire at 72 hours records garment comfort and tolerability and the participant's guess of allocation.

Sample size: based on Hill et al. (2017), a difference of 8.7 percentage points in MVC recovery at 72 hours (Cohen's d = 0.888), two-tailed alpha 0.05 and power 0.80 require 42 participants (21 per group); allowing approximately 20% dropout, 52 participants (26 per group) will be enrolled.

Analysis: the primary analysis is on the intention-to-treat population using a linear mixed-effects model with group, timepoint and group-by-timepoint interaction as fixed effects, pre-exercise baseline as a covariate and participant as a random effect. Secondary models are additionally adjusted for sex. Pre-specified sensitivity analyses examine hormonal status, and a per-protocol analysis includes participants meeting the wear-adherence threshold (mean of at least 16 hours per day with no day below 12 hours). Creatine kinase is log-transformed and reported as geometric mean ratios.

Being tested
Mineral-infused garment, Non-infused control garment, Muscle-damaging eccentric exercise (drop jumps)
Keywords
recovery garment, mineral-infused textile, far-infrared, compression garment, eccentric exercise, drop jump, maximal voluntary contraction, creatine kinase, healthy volunteers

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Mineral-infused garmentOther

    Also called Mineral-infused clothing

    Commercially available lower-limb garments (socks and leggings) with the manufacturer's proprietary mineral formulation incorporated into the textile by a post-manufacturing infusion process. Three new, unworn sets are issued per participant (one per recovery day). Worn during the drop-jump protocol and for at least 16 hours per day (approximately 8 hours waking and 8 hours overnight) for 72 hours; removed for each muscle function assessment and for washing and personal care.

  • Non-infused control garmentOther

    Also called Sham garment

    Socks and leggings identical in appearance, fabric construction, sizing and packaging to the active garment but manufactured without the mineral infusion. Same issue quantity and wear schedule as the active garment.

  • Muscle-damaging eccentric exercise (drop jumps)Other

    100 drop jumps performed as 5 sets of 20 repetitions from a standardised box height with standardised landing technique, 10 seconds between jumps and 2 minutes between sets, under one-to-one supervision on Day 1. Used as the experimental model of exercise-induced muscle damage in both arms.

Study groups in NCT07873866
Study groupRoleWhat they receive
Mineral-infused garmentExperimentalParticipants wear mineral-infused socks and leggings during the muscle-damaging exercise protocol and for a minimum of 16 hours per day throughout the 72-hour recovery period.
Receives: Other: Mineral-infused garment; Other: Muscle-damaging eccentric exercise (drop jumps)
Non-infused control garmentSham comparatorParticipants wear socks and leggings manufactured to the same specification, fabric, colour, sizing and packaging as the active garment but without the mineral infusion, on the same wear schedule.
Receives: Other: Non-infused control garment; Other: Muscle-damaging eccentric exercise (drop jumps)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in maximal voluntary isometric contraction (MVC) force of the knee extensors at 72 hours post-exercise

    Peak isometric force of the knee extensors of the dominant limb measured by fixed-frame dynamometry, expressed as a percentage of the participant's pre-exercise baseline value.

    Measured: Pre-exercise baseline and 72 hours post-exercise

Secondary outcomes (5)
  1. Change in maximal voluntary isometric contraction (MVC) force of the knee extensors at 0, 24 and 48 hours post-exercise

    Peak isometric force of the knee extensors of the dominant limb measured by fixed-frame dynamometry, expressed as a percentage of pre-exercise baseline.

    Measured: Pre-exercise baseline and 0, 24 and 48 hours post-exercise

  2. Change in squat jump peak force

    Bilateral peak force during a maximal squat jump measured on a dual force plate system, expressed relative to pre-exercise baseline.

    Measured: Pre-exercise baseline and 0, 24, 48 and 72 hours post-exercise

  3. Change in perceived muscle soreness (delayed onset muscle soreness)

    Muscle soreness rated on a 100 mm visual analogue scale (0 mm = no soreness, 100 mm = worst soreness imaginable; higher scores indicate a worse outcome) immediately after a single bodyweight squat to a fixed box height.

    Measured: Pre-exercise baseline and 0, 24, 48 and 72 hours post-exercise

  4. Garment tolerability: number of participants with garment-related skin reactions or adverse events

    Skin under the garment is visually inspected at each visit and any redness, irritation, pressure marking, swelling or broken skin is graded as none, mild, moderate or severe. Garment comfort and tolerability are also reported by participants in the Study Exit Questionnaire.

    Measured: From Day 1 (garment issue) to 72 hours post-exercise

  5. Blinding integrity: proportion of participants correctly identifying their allocated garment

    Participants are asked in the Study Exit Questionnaire whether they believe they wore the mineral-infused garment, the non-infused garment, or are not sure.

    Measured: 72 hours post-exercise

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Oct 2026
  2. Study startNov 2026 (estimated)
  3. Primary completionMar 2027 (estimated)
  4. Study completionApr 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Parallel groups
Model description
Two-arm, parallel-group design with 1:1 allocation, stratified by sex. Both arms complete the same muscle-damaging drop-jump protocol and the same assessment schedule; the arms differ only in the garment worn.
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
52 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07873866
Sponsor's protocol ID
SSG-26-020-001
Acronym
PERFICT
Status last verified
Oct 2026
First submitted
8 Oct 2026
Last updated
20 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: There is no plan to make individual participant data publicly available. A de-identified dataset is provided to the study funder at the end of the study, and summary results will be posted to ClinicalTrials.gov.

Publications

  • Hill J, Howatson G, van Someren K, Gaze D, Legg H, Lineham J, Pedlar C. The Effects of Compression-Garment Pressure on Recovery After Strenuous Exercise. Int J Sports Physiol Perform. 2017 Sep;12(8):1078-1084. doi: 10.1123/ijspp.2016-0380. Epub 2017 Jan 4.

    PubMed 28051341

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