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Effect of different compression values of knee-length stockings on reduction of nocturia

Effect of different compression values of knee-length stockings on reduction of nocturia : a randomized prospective crossover study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1072240084
Enrollment
30
Registered
2024-12-10
Start date
2024-12-10
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

Nocturia Nocturia, Compression stockings, Urinary Diary, Sleep Activity Quality of life

Interventions

1) Screening will be recruited through continence care professional. 2)The order in which to intervene is generated and randomised using Excel. 3) Subjects will wear the following from morning to eve
Randomized Controlled Trial, compreeion stockings for medical use,Weak pressure compreeion stockings, Regular knee-length socks

Sponsors

Mizoguchi Akiko
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Subjects must be 40 years of age or older, of either sex, resident in Japan, able to communicate in Japanese, have symptoms of nocturia, and not meet any of the exclusion criteria.

Exclusion criteria

Exclusion criteria: If you have been diagnosed with severe heart or kidney failure, poorly controlled diabetes or hypertension, sleep apnea, prostate enlargement, or brain disease such as stroke or Parkinson's disease. Patients taking calcium channel blockers (dihydropyridine calcium channel blockers) such as Amlodin, Norvasc, Adalat, Atelec, Calblock, or Coniel for treatment of hypertension or angina pectoris. Those who take sleeping pills or sleep supplements before bedtime. Patients with severe swelling of the lower extremities that makes it difficult to wear normal socks. Those who started a new treatment or started taking supplements within 1 month of the survey. Those who have skin lesions, neuropathy, or poor circulation in the lower extremities. Those who are prohibited by their physician from wearing knee-length compression stockings. Patients with malignant diseases Those who cannot wear knee socks for one week in a row. Those who have difficulty in checking whether they are wearing elastic knee socks or not. Those who have to stay awake at night for work. Those who do not have a smart phone Those who cannot wear a smart watch during the survey

Design outcomes

Primary

MeasureTime frame
Differences in hours of undisturbed sleep (HUS) from bedtime to first elimination at night due to differences in compression values

Secondary

MeasureTime frame
Differences in the number of nocturnal voidings, initial nocturnal voiding volume, nocturnal voiding duration, nocturnal voiding volume, subjective sleep status at night, sleep and activity status (sleep duration, waking time, REM sleep, shallow sleep, deep sleep and sleep score, number of steps taken during the day) and quality of life due to different wearing pressure values

Contacts

Public ContactAkiko Mizoguchi

Fukuoka International University of Health and Welfare

amizoguchi@s.takagigakuen.ac.jp+81-92-707-7569

Outcome results

None listed

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