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A study on the usefulness of oral mucosal massage for patients with xerostomia-Open-label randomized controlled trial-

A study on the usefulness of oral mucosal massage for patients with xerostomia-Open-label randomized controlled trial- - A study on the usefulness of oral mucosal massage for patients with xerostomia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000040751
Enrollment
60
Registered
2020-07-01
Start date
2020-07-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

xerostomia

Interventions

Oral mucosal massage group: Oral mucosal massage is performed at home three times after each meal for 8 weeks Extraoral massage group: Extraoral massage is performed at home three times after each mea

Sponsors

Gerodontology, Department of Oral Health Science, Faculty of Dental Medicine, Hokkaido University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Those who are 20 years of age or older at the time of obtaining consent 2. Those who are aware of dry mouth 3. Those who have 1 degree or more of clinical diagnostic criteria for dry mouth. 4. A person who, after receiving a sufficient explanation before participating in this research, has a sufficient understanding and obtained the informed consent of the person himself/herself.

Exclusion criteria

Exclusion criteria: 1. Those who have a clear cause of dry mouth and are capable of causal treatment 2. Those who have difficulty in performing extraoral massage or oral mucosal massage due to hand movement disorder due to rheumatoid arthritis or cognitive impairment 3. Those who have stomatitis at the oral mucosal massage site 4. Person who used moisturizer in oral cavity within 2 months 5. Any other person who the research director judges to be inappropriate as a research target person

Design outcomes

Primary

MeasureTime frame
Comparison of subjective improvement of dry mouth symptoms by visual analogue scale between two groups 8 weeks after the start of the study

Countries

Japan

Contacts

Public ContactTakae Abe

Faculty of Dental Medicine, Hokkaido University Gerodontology

yutaka8@den.hokudai.ac.jp+81-(0)11-706-4582

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026