Hand-held temple massager tested as drug-free stress relief for midlife women
NCT ID NCT07639658
First seen Jun 27, 2026 · Last updated Sep 04, 2026 · Updated 1 time
Summary
This study tests whether a non-electric, hand-held temple massager—used daily for 4 weeks with a special lotion and optional lavender aromatherapy—can lower stress, improve emotional wellbeing, sleep quality, and overall quality of life in women aged 35 to 65. Participants use the device at home for at least 5 minutes each day and answer surveys through a secure app. There is no placebo group; researchers compare how participants feel before and after the 4-week period.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Temple Massager System (hand-held mechanical massage device with body lotion and optional lavender aromatherapy)
- What this could lead to
- If it works, this could offer a simple, drug-free way to ease daily stress, tension headaches, and sleep troubles for women in midlife.
- What could go wrong
- This is a small, single-arm observational study with no placebo group, so results may be due to the placebo effect or natural changes over time. The device is a general wellness product, not a medical treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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68 people
The number who actually took part.
- Started
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Jun 2026
- Finished
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Jul 2026
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Women aged 35 to 65 who experience daily stress, anxiety, tension headaches, facial tension, or TMJ-related discomfort, with self-reported headache frequency of two or more per week. Participants must be in good general health, on stable medication regimens if applicable, able to use a personal smartphone or tablet, and willing to use the Temple Massager System daily for 4 weeks. Participants are recruited nationwide through wellness research participant pools, social media advertising, and targeted digital outreach to women in wellness communities.
- Ages
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35 to 65 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Female, aged 35-65 years old, inclusive * Self-reported experience of daily stress, anxiety, tension headaches, facial tension, or TMJ-related discomfort * Headache frequency of 2 or more per week (self-reported) * If taking any prescription medication including SSRIs, anxiolytics, sleep medications, hormonal therapies, or blood pressure medications, must be on a stable dose for at least 4 weeks prior to study enrollment and throughout the course of the study * In good general health at the time of screening (Investigator discretion) * Able to read and understand English * Able to read, understand, and provide informed consent * Able to use a personal smartphone or tablet and access the study platform for daily data entry * Able to receive shipment of the study product at an address within the United States * Willing and able to use the Temple Massager System daily for 4 weeks Exclusion Criteria: * No personal smartphone or tablet, no internet access, or unwilling to use the study platform * Known allergy or sensitivity to lavender oil, mango butter, shea butter, arnica, or St. John's Wort (Note: lavender sensitivity alone is not exclusionary; an aromatherapy sensitivity protocol applies) * Active skin infection or open wounds on the face or temple area * Diagnosed trigeminal neuralgia or other cranial nerve pathology * Diagnosed vascular issues affecting the head or face: temporal arteritis, aneurysm, or cerebrovascular malformations * Bleeding disorders: history of easy bruising or bleeding in the face/head area, or current use of prescribed blood thinners (anticoagulants) such as Warfarin or Eliquis * Any surgery on the jaw, temples, or face within the last 6 months * Active inflammation: current redness, swelling, or extreme tenderness specifically over the temple arteries * Current use of prescription headache medications (triptans, topiramate, muscle relaxants, beta-blockers for migraine prophylaxis, or other prescription medications taken primarily for headache management) * Participants currently taking any prescribed medication for sleep or anxiety must be on a stable dose (no dose changes within the past 30 days) to be eligible; participants not on a stable dose are excluded * Current participation in another interventional study * Diagnosed Generalized Anxiety Disorder (GAD) * Currently pregnant, planning to become pregnant during the study period, or breastfeeding * Planned surgical procedure during the study period * Significant illness, disease, or condition which, in the opinion of the Principal Investigator, may impact the ability to participate in the study or impact the study outcomes * Unlikely for any reason to be able to comply with the study or considered unsuited for participation by the Principal Investigator
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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MOQ Collective, Ltd.
Fairfax, California, 94930, United States
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