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Delayed Onset Muscle SorenessNCT06076356

Effects of Foam Roller Versus KT Tape on Delayed Onset Muscle Soreness

A study testing Foam Rolling and Kinesio Taping in people with Delayed Onset Muscle Soreness, run by Riphah International University at 1 site in Pakistan.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Objective of this study is to compare the effects of foam roller with KT tape on DOMS. The university going students will be divided in two groups, with one group receiving Kinesio Tape as intervention and other Foam Rolling as intervention. Read more about this study

Who is it for?
Ages 18 to 36 years, men onlyHealthy volunteers can take part
Conditions the study is for
Delayed Onset Muscle Soreness
What is being tested?
Foam Rolling and Kinesio Taping
Could I receive a placebo?
No, everyone receives an active treatment
How many people
24 participants
Where
1 sitePakistan
Study dates
15 Aug 2023to 31 Jan 2024
Phase
Interventional
Are there results?
None posted in the registry

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 36 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Individuals with normal BMI (18.5 to 25 Kg/m2)

Who cannot join

  • Individuals with history of metabolic or musculoskeletal disease.
  • Individuals with any recent acute injury.
  • Athletes exercising regularly and regular gymnasium going individuals.

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Riphah International University (RIU)

    Islamabad, Islamabad, 44000

Other trials in Pakistan

About this study

Objective of this study is to compare the effects of foam roller with KT tape on DOMS. The university going students will be divided in two groups, with one group receiving Kinesio Tape as intervention and other Foam Rolling as intervention. Pain and range of motion will be assessed before and after the intervention and the effects of both interventions will be compared.

Read the detailed description

Delayed Onset Muscle Soreness (DOMS) is a common phenomenon experienced after unaccustomed or intense physical activity, characterized by muscle discomfort, pain, and reduced range of motion. Various interventions have been conducted to alleviate DOMS symptoms, including the use of foam rollers and Kinesiology Tape (KT tape).

This randomized controlled clinical trial aims to compare the effects of foam roller and KT tape interventions on reducing DOMS and improving muscle recovery. The participants would go for a single session of High Intensity Interval Training (HIIT) to induce DOMS. Group-A participants would receive KT taping afterwards, while Group-B participants would receive foam rolling as intervention. Their effect would be measured using Visual Analog Scale (VAS), Tenderness Grading Scale, Knee Range of Motion (ROM) and Vertical Jump Height. This study delves into the applications and potential benefits of KT tape and foam roller in managing DOMS, shedding light on their effectiveness and how they can contribute to enhancing post-exercise recuperation and overall well-being.

Being tested
Foam Rolling, Kinesio Taping
Keywords
DOMS, Foam Rolling, HIIT, Kinesio Taping, Resistance Training

What participants receive

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

  • Foam RollingOther

    Foam Roller for 90 seconds over anterior (quadriceps) and posterior (hamstrings) aspect of thigh.

  • Kinesio TapingOther

    Kinesio taping over anterior (quadriceps) and posterior (hamstrings) aspect of thigh.

Study groups in NCT06076356
Study groupRoleWhat they receive
Group AActive comparatorFoam Rolling Group
Receives: Other: Foam Rolling
Group BActive comparatorKinesio Taping Group
Receives: Other: Kinesio Taping

What is being measured

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

  1. Pain (VAS Score)

    Pain will be measured using Visual Analog Scale (VAS) ranging from zero (0=no pain) to ten (10=worst pain).

    Measured: Baseline, after 24 hours, after 48 hours, and after 72 hours

  2. Tenderness

    Tenderness will be measured using Tenderness Grading Scale ranging from zero (0=no tenderness) to four (4=severe tenderness).

    Measured: Baseline, after 24 hours, after 48 hours, and after 72 hours

Secondary outcomes (2)
  1. Knee Range of Motion (Flexion)

    Range of motion will be measured using Universal Goniometer

    Measured: Baseline, after 24 hours, after 48 hours, and after 72 hours

  2. Vertical Jump Height

    Vertical Jump Height will be measured using Vertec.

    Measured: Baseline, after 24 hours, after 48 hours, and after 72 hours

Timeline

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

  1. First posted10 Oct 2023
  2. Study start15 Aug 2023
  3. Primary completion30 Nov 2023 (estimated)
  4. Study completion31 Jan 2024 (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
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Concurrent Parallel Randomized Clinical Trial
Masking
Single blind
Who is masked
Participant
Enrolment
24 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06076356
Sponsor's protocol ID
REC/01615 Maria Nawaz
Status last verified
Oct 2023
First submitted
4 Oct 2023
Last updated
13 Oct 2023
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Foam Rolling and Kinesio Taping in people with Delayed Onset Muscle Soreness, run by Riphah International University at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 13 Oct 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pain (VAS Score) (time frame: Baseline, after 24 hours, after 48 hours, and after 72 hours). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Oct 2023.

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