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Cognitive Performance in Healthy AdultsNCT07893886

Back Massage Before a Cognitive Task in Healthy Young Adults

A study testing Classical Back Massage, Passive Rest and No Additional Break in people with Cognitive Performance in Healthy Adults, run by DSW Ideis University at 1 site in Poland.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This study will compare a 15-minute back massage, 15 minutes of quiet rest, and no additional break before a mental task in healthy adults aged 18 to 27 years. Each participant will complete all three conditions in a random order at separate visits. Read more about this study

Who is it for?
Ages 18 to 27 yearsHealthy volunteers can take part
Conditions the study is for
Cognitive Performance in Healthy Adults
What is being tested?
Classical Back Massage, Passive Rest and No Additional Break
Could I receive a placebo?
No, everyone receives an active treatment
How many people
78 participants
Where
1 sitePoland
Study dates
Nov 2026to Mar 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

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 27 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Age 18 to 27 years and good general health.
  • Informed consent and ability to attend three visits.
  • Normal or corrected vision, understanding of Polish instructions, and ability to perform the computer task with the dominant hand.

Who cannot join

  • Neurological, psychiatric, or other conditions that may affect study participation or task performance.
  • Medications or substances affecting autonomic function.
  • Contraindications to massage, including relevant skin lesions or inflammation.
  • Failure to understand the task after repeated instruction or to complete calibration.
  • Cognitive or relaxation-focused nonpharmacological interventions within the previous three months, excluding recreational physical activity.
  • Caffeine or nicotine within four hours, or strenuous exercise within 12 hours before a visit; the visit may be rescheduled.

Trial locations and contacts

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

Maciej Lachowicz, PhD contact

+48 605 072 627

maciej.lachowicz@awf.wroc.pl

Poland1 site
  • Akademia Wychowania Fizycznego im. Polskich Olimpijczyków we Wrocławiu

    Wroclaw

    Maciej Lachowicz, PhD, +48 605 072 627, maciej.lachowicz@awf.wroc.pl

Other trials in Poland

About this study

Official title: Classical Massage as Preparation for a Cognitive Task: A Randomized Three-Condition Crossover Study

This study will compare a 15-minute back massage, 15 minutes of quiet rest, and no additional break before a mental task in healthy adults aged 18 to 27 years. Each participant will complete all three conditions in a random order at separate visits. The study will measure task accuracy, heart rate, skin conductance, and perceived workload to assess whether massage offers a benefit beyond rest.

Read the detailed description

This randomized crossover study includes three visits approximately two weeks apart. Task practice and individual calibration take place before a seated resting measurement. Participants then receive massage, rest lying face down, or proceed directly to the task. The TLoadDback task lasts 16 minutes at a fixed, individually calibrated pace. Physiological signals are recorded during rest and task performance. Participants complete the NASA-TLX questionnaire after the task.

Being tested
Classical Back Massage, Passive Rest, No Additional Break
Keywords
Massage, Cognitive Workload, TLoadDback

What participants receive

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

  • Classical Back MassageOther

    A 15-minute classical back massage while lying face down, delivered by trained personnel before TLoadDback.

  • Passive RestBehavioural

    A 15-minute quiet rest lying face down on the massage table without massage before TLoadDback.

  • No Additional BreakOther

    TLoadDback begins immediately after the seated resting baseline, without an additional 15-minute preparation period.

Study groups in NCT07893886
Study groupRoleWhat they receive
Sequence ABCExperimentalBack massage, passive rest, then no additional break; one condition per visit before TLoadDback.
Receives: Other: Classical Back Massage; Behavioral: Passive Rest; Other: No Additional Break
Sequence ACBExperimentalBack massage, no additional break, then passive rest; one condition per visit before TLoadDback.
Receives: Other: Classical Back Massage; Behavioral: Passive Rest; Other: No Additional Break
Sequence BACExperimentalPassive rest, back massage, then no additional break; one condition per visit before TLoadDback.
Receives: Other: Classical Back Massage; Behavioral: Passive Rest; Other: No Additional Break
Sequence BCAExperimentalPassive rest, no additional break, then back massage; one condition per visit before TLoadDback.
Receives: Other: Classical Back Massage; Behavioral: Passive Rest; Other: No Additional Break
Sequence CABExperimentalNo additional break, back massage, then passive rest; one condition per visit before TLoadDback.
Receives: Other: Classical Back Massage; Behavioral: Passive Rest; Other: No Additional Break
Sequence CBAExperimentalNo additional break, passive rest, then back massage; one condition per visit before TLoadDback.
Receives: Other: Classical Back Massage; Behavioral: Passive Rest; Other: No Additional Break

What is being measured

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

  1. Weighted Accuracy on TLoadDback (WAcc)

    Weighted accuracy across the full task: 0.65 x letter accuracy + 0.35 x digit accuracy. Letter accuracy includes correct detections and correct withholding of responses; digit accuracy is correct parity classification. Scores range from 0 to 100%, with higher scores indicating better performance.

    Measured: During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).

  2. Mean Heart Rate During TLoadDback

    Mean heart rate in beats per minute during the task, derived from photoplethysmography. Analyses will account for the precondition resting baseline from the same visit.

    Measured: During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).

  3. Mean Skin Conductance During TLoadDback

    Mean skin conductance in microsiemens during the task. Analyses will account for the precondition resting baseline from the same visit.

    Measured: During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).

Secondary outcomes (2)
  1. Perceived Workload (NASA-TLX)

    Unweighted mean of six NASA-TLX ratings, each scored from 0 to 100 and oriented so that higher values indicate greater workload or poorer perceived performance.

    Measured: Immediately after the task at each of three visits approximately two weeks apart (about four weeks in total).

  2. Median Response Time on TLoadDback

    Median response time, in milliseconds, for correct responses that require a key press during the task.

    Measured: During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).

Timeline

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

  1. First posted26 Oct 2026
  2. Study startNov 2026 (estimated)
  3. Primary completionMar 2027 (estimated)
  4. Study completionMar 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
Crossover
Model description
Each participant completes three conditions in one of six randomized sequences: ABC, ACB, BAC, BCA, CAB, or CBA. A: back massage; B: passive rest; C: no additional break. Visits are approximately two weeks apart.
Masking
None (open label)
Enrolment
78 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07893886
Sponsor's protocol ID
COG-MASS-2026-01
Status last verified
Oct 2026
First submitted
18 Oct 2026
Last updated
26 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: No individual participant data sharing plan has been established. Study results will be reported in aggregate.

Questions about this trial

What is this clinical trial studying?

A study testing Classical Back Massage, Passive Rest and No Additional Break in people with Cognitive Performance in Healthy Adults, run by DSW Ideis University at 1 site in Poland.

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 3 inclusion and 6 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: opening soon, as of the sponsor's last update on 26 Oct 2026. 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 Poland. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Maciej Lachowicz, PhD (+48 605 072 627, maciej.lachowicz@awf.wroc.pl), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Weighted Accuracy on TLoadDback (WAcc) (time frame: During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).). The study lists 3 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 26 Oct 2026.

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