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Nocturnal Leg Cramps in Geneva : an Observational Study

Prevalence, Main Features and Treatment of Nocturnal Leg Cramps in Geneva: A Primary Care Prospective Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02548507
Acronym
CNMI
Enrollment
129
Registered
2015-09-14
Start date
2015-03-31
Completion date
2018-04-30
Last updated
2018-05-22

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

Conditions

Nocturnal Leg Cramps, Sleep Wake Transition Disorders

Brief summary

Background : Nocturnal leg cramps (NLC) are defined as painful involuntary contractions of the lower limbs occurring during prolonged periods of rest, typically during the night. They may cause severe pain and sleep disturbance, and are particularly common among older adults, though they can occur in all decades of life. They are frequently unreported to physicians. To the investigators' knowledge, no epidemiological studies have been conducted in Switzerland, but in a general population survey carried out in the UK (n=233), the overall prevalence of NLC was 37% and the disorder was more prevalent in older subjects (\>80 years old: 54%). Of those who experienced NLC, 40% had cramps three or more times per week and 6% nightly. Another study performed in older US veterans (n=515) showed that 56% suffered from NLC. The precise cause of these cramps is unclear. Most NLC occurring in adults appear to be idiopathic, but potential contributing factors include low levels of certain minerals, extracellular fluid volume depletion and prolonged sitting or inappropriate leg position during sedentary activity. Research question : What are the prevalence and the main features of NLC in patients consulting primary care physicians (PCPs) in Geneva, and how do PCPs treat this affection? Primary objective : To compute the prevalence of NLC in patients consulting PCPs in Geneva, explore its main features (number, duration, severity and sleep disturbance) and assess how PCPs treat this affection. Study design : Prospective observational study using questionnaire and daily log completed by patients.

Interventions

Sponsors

University of Geneva, Switzerland
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients of 50 years old or more, * currently presenting NLC (The definition of NLC used for the purpose of the study is any cramp in the legs or feet, occurring during the sleep (eg long rest) period). * coming to the practice for a planned consultation.

Exclusion criteria

* Patients suffering from a terminal illness * from disorders affecting their ability to consent, * not speaking French * or not having a telephone.

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of NLCPresence or absence of NLC will be checked during the time of recruitment for each participant PCP, with expected average of 1 to 6 months.In order to compute the prevalence of NLC, the PCPs will be asked to specify for each patient coming for a planned consultation whether he/she has NLC, meets the inclusion criteria and accept to participate (group 1), has NLC, meets the inclusion criteria but refuses to participate (group 2) or has NLC but does not meet the inclusion criteria (group 3). For patients in the group 1 doctors will record the current date, the name and the first name, the gender, the date of birth and the phone number; for patients in the group 2 they will record the current date, the gender and the date of birth; and finally for patients in the group 3 they will record the current date, the gender, the date of birth and the exclusion criterion.

Secondary

MeasureTime frameDescription
Duration of nocturnal leg crampsDuring two weeks after recruitmentVoluntaries will record during two weeks the duration of cramps in a daily log.
Severity of pain related with nocturnal leg crampsDuring two weeks after recruitmentVoluntaries will record the severity of cramps in a daily log, standardized on an analog numerical scale of 1 to 10 .
Severity of sleep disturbance related with nocturnal leg crampsDuring two weeks after recruitmentVoluntaries will record the severity of sleep disturbance related with NLC, in a daily log, standardized on an analog numerical scale of 1 to 10.
Frequency of NLCDuring two weeks after recruitmentVoluntaries will record during two weeks the number of cramps in a daily log.
Patient quality of life1 year after initial recruitmentVoluntaries will fill a SF36 questionnaire
Patient quality of sleep1 year after initial recruitmentVoluntaries will fill a PSQI questionnaire
Patient expectancies for nocturnal leg cramps treatmentTwo weeks after recruitmentWe will ask the voluntaries to specify the average pain and sleep disturbance related with NLC on analog numerical scale of 1 to 10. We'll then ask them what improvement they would expect from a treatment on the same analog numeric scale for pain and sleep disturbance.

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026