Condition 1: Anxiety. Condition 2: Sleep Quality. Other anxiety disorders
Conditions
Interventions
Intervention 1: Intervention group: In both groups, prior to the intervention, all necessary measures such as maintaining patient privacy and establishing appropriate verbal communication will be obs
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Full consciousness and orientation to time and place Ability to read, write, and communicate effectively Informed consent to participate in the study (31) Absence of psychotic symptoms (such as hallucinations and delusions) based on the psychiatrist’s diagnosis recorded in the patient’s medical file No use of medications that directly affect sleep or anxiety Healthy and intact skin on the lower limbs (32)
Exclusion criteria
Exclusion criteria: Presence of severe or chronic illnesses that prevent participation in the intervention (e.g., severe heart failure). Presence of severe skin disorders or open wounds in the lower limbs Use of medications affecting sleep or anxiety prior to enrollment in the study Diagnosis of psychosis or presence of hallucinations and delusions by a psychiatrist Inability to read, write, or communicate verbally. Lack of informed consent to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Anxiety. Timepoint: The outcome was measured before the intervention and immediately after the intervention. Method of measurement: Spielberger Questionnaire.;Sleep Quality. Timepoint: The outcome was measured before the intervention and immediately after the intervention. Method of measurement: The Pittsburgh Sleep Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahya Torkaman
Kerman University of Medical Sciences
Outcome results
None listed