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effect of local heat on restless legs syndrome and excessive fatigue in nurses

The effect of local heat on restless legs syndrome and excessive fatigue in nurses working in the intensive care unit

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190723044316N1
Enrollment
120
Registered
2019-10-10
Start date
2019-10-12
Completion date
Unknown
Last updated
2019-11-05

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

Conditions

Condition 1: Restless leg syndrome. Condition 2: . Restless legs syndrome

Interventions

Intervention 1: Intervention group: The intervention of the experimental group will be conducted for 4 weeks in 12 sessions. After the end of the intervention the post-test will be taken and the quest

Sponsors

Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Having a year of experience Undergraduate degree Restless leg syndrome Physicians working in intensive care units

Exclusion criteria

Exclusion criteria: Taking Medication and Supplements People taking painkillers and opiates within 72 hours before the study Consumers of psychotropic drugs Neuromuscular disorders and arthritis Pregnant women Wounds and redness of the limbs Heat sensitivity Vascular diseases and diabetes

Design outcomes

Primary

MeasureTime frame
One of the variables in this study is restless legs syndrome. To this end, the International Standard Questionnaire for Restless Legs Syndrome will be provided to nurses by intensive care unit. Timepoint: The intervention of the experimental group will be done for 4 weeks in 12 sessions. Method of measurement: The intervention of the experimental group will be done for 4 weeks in 12 sessions after the end of the intervention the post-test will be re-tested and again the questionnaires will be completed by the test and control group and the results will be compared with the previous results.;One of the variables of this study is excessive fatigue and for this purpose Smyths Fatigue Inventory (MFI) will be provided to the nurses of intensive care units. Timepoint: The intervention of the experimental group will be done for 4 weeks in 12 sessions. Method of measurement: The intervention of the experimental group will be done for 4 weeks in 12 sessions after the end of the intervention the post-test will be re-tested and again the questionnaires will be completed by the test and control group and the results will be compared with the previous results.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Ameri

Shahroud University of Medical Sciences

maryam19_2006@yahoo.com+98 23 3239 5054

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 11, 2026