Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

Back Massage Before a Cognitive Task in Healthy Young Adults

9 de noviembre de 2026 actualizado por: DSW Ideis University

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.

Descripción general del estudio

Estado

Aún no reclutando

Condiciones

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

78

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

      • Wroclaw, Polonia
        • Akademia Wychowania Fizycznego im. Polskich Olimpijczyków we Wrocławiu
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 27 años (Adulto)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • 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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Ciencia básica
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Sequence ABC

Back massage, passive rest, then no additional break; one condition per visit before TLoadDback.

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

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

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

Experimental: Sequence ACB

Back massage, no additional break, then passive rest; one condition per visit before TLoadDback.

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

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

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

Experimental: Sequence BAC

Passive rest, back massage, then no additional break; one condition per visit before TLoadDback.

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

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

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

Experimental: Sequence BCA

Passive rest, no additional break, then back massage; one condition per visit before TLoadDback.

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

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

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

Experimental: Sequence CAB

No additional break, back massage, then passive rest; one condition per visit before TLoadDback.

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

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

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

Experimental: Sequence CBA

No additional break, passive rest, then back massage; one condition per visit before TLoadDback.

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

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

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

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Weighted Accuracy on TLoadDback (WAcc)
Periodo de tiempo: During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).

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.

During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).
Mean Heart Rate During TLoadDback
Periodo de tiempo: During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).

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.

During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).
Mean Skin Conductance During TLoadDback
Periodo de tiempo: During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).

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

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

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Perceived Workload (NASA-TLX)
Periodo de tiempo: Immediately after the task at each of three visits approximately two weeks apart (about four weeks in total).

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.

Immediately after the task at each of three visits approximately two weeks apart (about four weeks in total).
Median Response Time on TLoadDback
Periodo de tiempo: During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).

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

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

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Letter Accuracy on TLoadDback
Periodo de tiempo: During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).

Percentage of correct letter trials, including correct detections of repeated letters and correct withholding of responses to nonrepeated letters. Higher values indicate better performance.

During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).
Digit Accuracy on TLoadDback
Periodo de tiempo: During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).

Percentage of correctly classified digit-parity trials. Scores range from 0 to 100%, with higher values indicating better performance.

During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).
Incorrect Responses on TLoadDback
Periodo de tiempo: During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).

Number of incorrect responses during the task. Higher counts indicate more errors.

During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).
Omitted Required Responses on TLoadDback
Periodo de tiempo: During the 16-minute task at each of three visits approximately two weeks apart (about four weeks in total).

Number of trials with no response when a response is required. Correct withholding of a response to a nonrepeated letter is not counted as an omission.

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

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Maciej Lachowicz, PhD, Akademia Wychowania Fizycznego im. Polskich Olimpijczyków we Wrocławiu

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de noviembre de 2026

Finalización primaria (Estimado)

1 de marzo de 2027

Finalización del estudio (Estimado)

1 de marzo de 2027

Fechas de registro del estudio

Enviado por primera vez

18 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

18 de octubre de 2026

Publicado por primera vez (Actual)

26 de octubre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

12 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

9 de noviembre de 2026

Última verificación

1 de octubre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • COG-MASS-2026-01

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

No individual participant data sharing plan has been established. Study results will be reported in aggregate.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Suscribir