InsomniaautosleepilotNCT06788288
The Long-term Impact of Massage Chairs on Sleep Quality.
A study testing Massage Chair session and Washout period in people with Insomnia, run by University of Thessaly at 1 site in Greece.
Trial summary
Modern technology is reshaping the massage industry, improving relaxation and well-being with pioneering devices. The automatic massage chairs stand as a testament to this evolution, integrating ergonomic design with advanced massage techniques to facilitate deep tissue relaxation, and sleep quality and enhance… Read more about this study
- Who is it for?
- Ages 18 to 45 years
- Conditions the study is for
- Insomnia
- What is being tested?
- Massage Chair session and Washout period
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 20 participants
- Where
- 1 siteGreece
- Study dates
- 4 Mar 2024to 31 Dec 2025
- 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 45 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- score of ≥16 on the Athens Insomnia Scale (AIS-8)
Who cannot join
- history of mental illness,
- history of epilepsy
- acute or chronic condition that would limit the ability of the patient to participate in the study
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Greece1 site, 1 recruiting
- Recruiting
School of Physical Education, Sports and Dietetics, TEFAA
Trikala, Thessaly, GR42100
Christina Karatzaferi, PhD, +302431047015 ext. 7015, ck@uth.gr
Ioannis Stefanidis, MD, PhD, +30-2110681667 ext. 1667, stefanid@uth.gr
About this study
Official title: The Long-term Impact of the Usage of New Generation Massage Chairs on Quality and Quantity of Sleep-in Individuals Suffering from Insomnia.
Modern technology is reshaping the massage industry, improving relaxation and well-being with pioneering devices. The automatic massage chairs stand as a testament to this evolution, integrating ergonomic design with advanced massage techniques to facilitate deep tissue relaxation, and sleep quality and enhance overall well-being.
Aim: The aim of the current study is to assess the long-term impact of the new generations of massage chairs prior to bed-time in aspects related to sleep and quality of life in individuals with severe symptoms of insomnia.
Read the detailed description
Study Design The current study will assess the impact of daily usage (30 consecutive automatic massage sessions) of deep relaxation full body massage sessions using the 4D new generations' massage chairs in individuals suffering from insomnia. The massage chair will be located in patients' house/bedroom during the whole trial period.
Participants will follow a crossover design with one-month interval period for three months in total. Participants will be randomly assigned into two equal-sized groups receiving the intervention (massage) following a distinct pattern: for the Group-1: one month on, one month off, one month on, and for Group_2: one month off, one month on, one month off. During the "on" period, massage chair is located at participant's house while during the "off" period, massage chair is removed from participant's house.
During the "on" periods, participants could use the massage chair prior to bed time (last action before sleeping) and select from one of twelve programmed relaxation massage options. They were required to use the chair for at least 30 minutes daily, primarily before going to bed. The study was approved by the Human Research and Ethics Committee of the University of Thessaly (2334-5/4-2/7.2.2024). All Subjects gave their written informed consent prior to study participation.
Procedure All measurements will be conducted at the participants' own homes. Massage sessions will be performed in the participants' home prior to bedtime, utilizing the automatic massage chair provided during the study period.
The initial screening requires that all participants score ≥16 on the Athens Insomnia Scale (AIS-8). The Pittsburgh Sleep Quality Index (PSQI) was provided for participants to complete every 30 days over the three-month period. Additionally, during the first visit, all participants completed a series of validated questionnaires assessing quality of life, depression score, sleep quality, stress, and general fatigue. The same questionnaires were also completed during the final visit. After each visit and immediately after the completion of the 30 min automatic massage, participants will be connected to the portable polysomnography system and they will stay alone to follow their bedtime routine. The study recording will be completed when the participant wakes up and disconnects the system.
Questionnaires The following questionnaires will be administered using the interview method by experienced researchers.
- The Athens Insomnia Scale 1 and the Pittsburgh Sleep Quality Index (PSQI) will be used to assess sleep quality and the existence of any sleep abnormalities.
- The Short Form survey 36-item 36 quality of life questionnaire (SF-36) will be used to assess the health-related quality of life.
- The Beck Depression Inventory (BDI) questionnaire will be used for the assess symptoms of depression.
- The Perceived Stress Scale (PSS) will be used to assess the stress levels.
Body Composition Body composition will be assessed using anthropometric measurements, including BMI and bioelectrical impedance analysis with a Tanita DC-360S device (Tanita Corporation, Tokyo, Japan), following standard methodology.
Sleep Assessment A portable sleep monitoring system will be used to assess sleep quality and quantity (Home Sleep Test, Somnomedics, GmbH, Germany). The system records EEG, EOG, and EMG signals overnight. EEG data will be analyzed in 30-second epochs using SomnoMedics PSG analysis software (Domino panel ver. 3.0.0.8) with manual editing. The HomeSleepTest REM+ device will be used for PSG, with electrodes placed according to the 10/20 system on key brain regions: Fp1 (left) and M1 for EEG, and near the eyes for EOG. This setup ensures accurate monitoring of sleep architecture and high-fidelity recordings of brain activity and eye movements.
Analysis of the sleep study will be reported as follows: Total Sleep Time (total amount of sleep time scored during the total recording time); Sleep Efficiency (Total sleep time/Time in bed); Sustained Sleep Efficiency (Total sleep time/(Time in bed - Sleep laten-cy stage 2); Sleep Latency (the period of time it takes for a person to fall asleep after they have gone to bed and tried to initiate sleep); Sleep Latency N1 (the period of time between wakefulness and when sleep begins); Sleep Latency N2 (the period of time between time in bed and sleep onset stage 2); REM Latency (the amount of time elapsed between the onset of sleep to the first REM stage).
Massage Session Automatic Electric Massage Chair (AEMC) The Z1 Full Body 4D Massage Chair (Z1-SL Massage Chair, China, www.back2life.gr) will be used in the current study. The Z1-SL chair features a curved rail mechanism for both S-shaped (horizontal) and L-shaped (vertical) massages, covering areas from the head down toes. It includes 58 air cushions for air compression massage, while intelligent mechanical arms, rotating 360°, follow the body's contour, scanning and targeting specific areas for treatment.
The chair integrates a 4D massage system with professional techniques such as kneading, tapping, shiatsu, stretching, air compression, roller, and thermal massage. These techniques allow multidimensional effects in width, length, and depth, tailored to individual needs. Twelve automated programs vary in intensity, and the roller mechanism adjusts to body widths of 3 to 22 cm for focused application to areas like the cervical spine, back, and lower back.
The chair's infrared preheating function (carbon fiber-based) enhances relaxation and circulation by heating the back, pelvis, and thighs. This feature, combined with an extendable foot section and an airbag/roller system, ensures comfort for individuals of different sizes, providing muscle relaxation, fatigue relief, and improved blood circulation.
- Conditions
- Insomnia
- Being tested
- Massage Chair session, Washout period
- Keywords
- poor sleepers, stress, fatigue
- Medical subject headings
- Sleep Initiation and Maintenance Disorders, Fatigue
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Massage Chair sessionOther
Also called Automatic Electric Massage chair
The intervention is composed of a full-body relaxation massage offered by an automatic electric massage chair. The intervention will last for 3 months while the participant will change between massage and washout periods.
Washout periodOther
Also called no intervention
During this phase, participants will spend on month without any intervention (massage) accounting for a washout period.
| Study group | Role | What they receive |
|---|---|---|
| Group 1 - On-Off-On | Experimental | Participants will follow a crossover design with a one-month interval period for three months in total. Participants will be randomly assigned into two equal-sized groups receiving the intervention (massage) following a distinct pattern: for the Group-1: one month on, one month off, one month on. During the "on" period, the massage chair will be located at the participant's house while during the "off" period, the massage chair will be removed from the participant's house (washout period). Receives: Other: Massage Chair session; Other: Washout period |
| Group 2 - Off-On-Off | Experimental | Participants will follow a crossover design with a one-month interval period for three months in total. Participants will be randomly assigned into two equal-sized groups receiving the intervention (massage) following a distinct pattern: for the Group-2: one month off, one month on, one month off. During the "on" period, the massage chair will be located at the participant's house while during the "off" period, the massage chair will be removed from the participant's house (washout period). Receives: Other: Massage Chair session; Other: Washout period |
What is being measured
The primary outcome is the main question the study is designed to answer.
Sleep Efficiency
Total sleep time over Time spend in bed
Measured: At baseline, after each month and at the end of the 3 months period.
Insomnia Score
For the calculation of the Insomnia score, the Athens Insomnia Scale (AIS-8) will be used. The score ranges from 0 - 24 with a higher number implying worse insomnia symptoms.
Measured: At baseline, after each month and at the end of the 3 months period.
Secondary outcomes (1)
Sleep Quality Score
The Pittsburgh Sleep Quality Index (PSQI) will be used to assess sleep quality and the existence of any sleep abnormalities. The score ranges from 0 - 21 with a higher score implying worse sleep quality.
Measured: At baseline, after each month and at the end of the 3 months period.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Jan 2025
- Study start4 Mar 2024
- Primary completion15 Dec 2025 (estimated)
- Study completion31 Dec 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for InsomniaStudies of the same condition, open and under way.
- More trials run by University of ThessalyThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Supportive care
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 20 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Thessaly
- Sponsor type
- University, hospital or other
- Collaborators
- University of Nicosia
- Responsible party
- Principal investigator, Giorgos K. Sakkas, University of Thessaly
- Investigators
- Giorgos Sakkas, PhD, Study chair, University of Thessaly
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06788288
- Sponsor's protocol ID
- 2334-5/4-2/7.2.2024
- Acronym
- autosleepilot
- Status last verified
- Jan 2025
- First submitted
- 16 Jan 2025
- Last updated
- 27 Jan 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: When the data are available, we will provide a link to the data at the ClinicalTrials.gov record in the Available IPD/Information field in the References module of the Protocol Section.
Publications
Xie J, Fu M, Liu T, Li S, Liu G, Wang J, Ji C, Zhang T. Clinical studies on the electric automatic massage therapy for recovery of acute sports fatigue. Technol Health Care. 2023;31(S1):185-197. doi: 10.3233/THC-236016.
PubMed 37038791Kim JW, Lim AR, Lee JY, Lee JY, Lee S, Choi YJ, Kim YH, Park KH. The clinical effect of an electric massage chair on chemotherapy-induced nausea and vomiting in cancer patients: randomized phase II cross-over trial. BMC Complement Med Ther. 2024 Apr 19;24(1):163. doi: 10.1186/s12906-024-04464-8.
PubMed 38641782Khairudin MN, Vallikkannu N, Gan F, Hamdan M, Tan PC. Electric massage chairs reduce labor pain in nulliparous patients: a randomized crossover trial. Am J Obstet Gynecol MFM. 2024 Apr;6(4):101324. doi: 10.1016/j.ajogmf.2024.101324. Epub 2024 Mar 4.
PubMed 38447674
Study at a glance
From the registry record, last updated by the sponsor on 27 Jan 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Long-term Impact of the Usage of New Generation Massage Chairs on Quality and Quantity of Sleep-in Individuals Suffering from Insomnia.
- ClinicalTrials.gov ID
- NCT06788288
- Acronym / sponsor ID
- autosleepilot / 2334-5/4-2/7.2.2024
- Conditions
- Insomnia
- Keywords
- poor sleepers, stress, fatigue
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 20 participants (estimated)
- Lead sponsor
- University of ThessalyUniversity, hospital or other
- Collaborators
- University of Nicosia
- Study start
- 4 Mar 2024 (actual)
- Primary completion
- 15 Dec 2025 (estimated)
- Study completion
- 31 Dec 2025 (estimated)
- First posted
- 23 Jan 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Modern technology is reshaping the massage industry, improving relaxation and well-being with pioneering devices. The automatic massage chairs stand as a testament to this evolution, integrating ergonomic design with advanced massage techniques to facilitate deep tissue relaxation, and sleep quality and enhance overall well-being.
Aim: The aim of the current study is to assess the long-term impact of the new generations of massage chairs prior to bed-time in aspects related to sleep and quality of life in individuals with severe symptoms of insomnia.
Detailed description
Study Design The current study will assess the impact of daily usage (30 consecutive automatic massage sessions) of deep relaxation full body massage sessions using the 4D new generations' massage chairs in individuals suffering from insomnia. The massage chair will be located in patients' house/bedroom during the whole trial period.
Participants will follow a crossover design with one-month interval period for three months in total. Participants will be randomly assigned into two equal-sized groups receiving the intervention (massage) following a distinct pattern: for the Group-1: one month on, one month off, one month on, and for Group_2: one month off, one month on, one month off. During the "on" period, massage chair is located at participant's house while during the "off" period, massage chair is removed from participant's house.
During the "on" periods, participants could use the massage chair prior to bed time (last action before sleeping) and select from one of twelve programmed relaxation massage options. They were required to use the chair for at least 30 minutes daily, primarily before going to bed. The study was approved by the Human Research and Ethics Committee of the University of Thessaly (2334-5/4-2/7.2.2024). All Subjects gave their written informed consent prior to study participation.
Procedure All measurements will be conducted at the participants' own homes. Massage sessions will be performed in the participants' home prior to bedtime, utilizing the automatic massage chair provided during the study period.
The initial screening requires that all participants score ≥16 on the Athens Insomnia Scale (AIS-8). The Pittsburgh Sleep Quality Index (PSQI) was provided for participants to complete every 30 days over the three-month period. Additionally, during the first visit, all participants completed a series of validated questionnaires assessing quality of life, depression score, sleep quality, stress, and general fatigue. The same questionnaires were also completed during the final visit. After each visit and immediately after the completion of the 30 min automatic massage, participants will be connected to the portable polysomnography system and they will stay alone to follow their bedtime routine. The study recording will be completed when the participant wakes up and disconnects the system.
Questionnaires The following questionnaires will be administered using the interview method by experienced researchers.
- The Athens Insomnia Scale 1 and the Pittsburgh Sleep Quality Index (PSQI) will be used to assess sleep quality and the existence of any sleep abnormalities.
- The Short Form survey 36-item 36 quality of life questionnaire (SF-36) will be used to assess the health-related quality of life.
- The Beck Depression Inventory (BDI) questionnaire will be used for the assess symptoms of depression.
- The Perceived Stress Scale (PSS) will be used to assess the stress levels.
Body Composition Body composition will be assessed using anthropometric measurements, including BMI and bioelectrical impedance analysis with a Tanita DC-360S device (Tanita Corporation, Tokyo, Japan), following standard methodology.
Sleep Assessment A portable sleep monitoring system will be used to assess sleep quality and quantity (Home Sleep Test, Somnomedics, GmbH, Germany). The system records EEG, EOG, and EMG signals overnight. EEG data will be analyzed in 30-second epochs using SomnoMedics PSG analysis software (Domino panel ver. 3.0.0.8) with manual editing. The HomeSleepTest REM+ device will be used for PSG, with electrodes placed according to the 10/20 system on key brain regions: Fp1 (left) and M1 for EEG, and near the eyes for EOG. This setup ensures accurate monitoring of sleep architecture and high-fidelity recordings of brain activity and eye movements.
Analysis of the sleep study will be reported as follows: Total Sleep Time (total amount of sleep time scored during the total recording time); Sleep Efficiency (Total sleep time/Time in bed); Sustained Sleep Efficiency (Total sleep time/(Time in bed - Sleep laten-cy stage 2); Sleep Latency (the period of time it takes for a person to fall asleep after they have gone to bed and tried to initiate sleep); Sleep Latency N1 (the period of time between wakefulness and when sleep begins); Sleep Latency N2 (the period of time between time in bed and sleep onset stage 2); REM Latency (the amount of time elapsed between the onset of sleep to the first REM stage).
Massage Session Automatic Electric Massage Chair (AEMC) The Z1 Full Body 4D Massage Chair (Z1-SL Massage Chair, China, www.back2life.gr) will be used in the current study. The Z1-SL chair features a curved rail mechanism for both S-shaped (horizontal) and L-shaped (vertical) massages, covering areas from the head down toes. It includes 58 air cushions for air compression massage, while intelligent mechanical arms, rotating 360°, follow the body's contour, scanning and targeting specific areas for treatment.
The chair integrates a 4D massage system with professional techniques such as kneading, tapping, shiatsu, stretching, air compression, roller, and thermal massage. These techniques allow multidimensional effects in width, length, and depth, tailored to individual needs. Twelve automated programs vary in intensity, and the roller mechanism adjusts to body widths of 3 to 22 cm for focused application to areas like the cervical spine, back, and lower back.
The chair's infrared preheating function (carbon fiber-based) enhances relaxation and circulation by heating the back, pelvis, and thighs. This feature, combined with an extendable foot section and an airbag/roller system, ensures comfort for individuals of different sizes, providing muscle relaxation, fatigue relief, and improved blood circulation.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Group 1 - On-Off-On | Experimental | Other: Massage Chair session, Other: Washout periodParticipants will follow a crossover design with a one-month interval period for three months in total. Participants will be randomly assigned into two equal-sized groups receiving the intervention (massage) following a distinct pattern: for the Group-1: one month on, one month off, one month on. During the "on" period, the massage chair will be located at the participant's house while during the "off" period, the massage chair will be removed from the participant's house (washout period). |
| Group 2 - Off-On-Off | Experimental | Other: Massage Chair session, Other: Washout periodParticipants will follow a crossover design with a one-month interval period for three months in total. Participants will be randomly assigned into two equal-sized groups receiving the intervention (massage) following a distinct pattern: for the Group-2: one month off, one month on, one month off. During the "on" period, the massage chair will be located at the participant's house while during the "off" period, the massage chair will be removed from the participant's house (washout period). |
Who may qualify
- Ages
- 18 to 45 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (1 listed)
- score of ≥16 on the Athens Insomnia Scale (AIS-8)
Key exclusion criteria (3 listed)
- history of mental illness,
- history of epilepsy
- acute or chronic condition that would limit the ability of the patient to participate in the study
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Massage Chair sessionAlso: Automatic Electric Massage chairThe intervention is composed of a full-body relaxation massage offered by an automatic electric massage chair. The intervention will last for 3 months while the participant will change between massage and washout periods. | Other | Group 1 - On-Off-On, Group 2 - Off-On-Off |
| Washout periodAlso: no interventionDuring this phase, participants will spend on month without any intervention (massage) accounting for a washout period. | Other | Group 1 - On-Off-On, Group 2 - Off-On-Off |
Primary outcome
Sleep Efficiency
Time frame: At baseline, after each month and at the end of the 3 months period.
Total sleep time over Time spend in bed
Insomnia Score
Time frame: At baseline, after each month and at the end of the 3 months period.
For the calculation of the Insomnia score, the Athens Insomnia Scale (AIS-8) will be used. The score ranges from 0 - 24 with a higher number implying worse insomnia symptoms.
1 secondary outcome
Sleep Quality Score
Time frame: At baseline, after each month and at the end of the 3 months period.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Jan 2025.
- Background: PubMed 37038791Xie J, Fu M, Liu T, Li S, Liu G, Wang J, Ji C, Zhang T. Clinical studies on the electric automatic massage therapy for recovery of acute sports fatigue. Technol Health Care. 2023;31(S1):185-197. doi: 10.3233/THC-236016.
- Background: PubMed 38641782Kim JW, Lim AR, Lee JY, Lee JY, Lee S, Choi YJ, Kim YH, Park KH. The clinical effect of an electric massage chair on chemotherapy-induced nausea and vomiting in cancer patients: randomized phase II cross-over trial. BMC Complement Med Ther. 2024 Apr 19;24(1):163. doi: 10.1186/s12906-024-04464-8.
- Background: PubMed 38447674Khairudin MN, Vallikkannu N, Gan F, Hamdan M, Tan PC. Electric massage chairs reduce labor pain in nulliparous patients: a randomized crossover trial. Am J Obstet Gynecol MFM. 2024 Apr;6(4):101324. doi: 10.1016/j.ajogmf.2024.101324. Epub 2024 Mar 4.
- Individual participant dataSharing planned: Yes. When the data are available, we will provide a link to the data at the ClinicalTrials.gov record in the Available IPD/Information field in the References module of the Protocol Section.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Giorgos Sakkas, PhD study chair
University of Thessaly
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Massage Chair session and Washout period in people with Insomnia, run by University of Thessaly at 1 site in Greece.
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: looking for participants now, as of the sponsor's last update on 27 Jan 2025. 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 Greece. 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 Giorgos Sakkas, PhD (+30-24310 47022 ext. 7022, gsakkas@uth.gr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Sleep Efficiency (time frame: At baseline, after each month and at the end of the 3 months period.). 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?
On the ClinicalTrials.gov record for NCT06788288, which also lists 3 linked publications.
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 27 Jan 2025.