Skip to content

Effect of progressive muscle relaxation technique on postoperative pain sleep quality, and anxiety in hospitalized patients with hip fractures

Examining the effect of progressive muscle relaxation technique on postoperative pain, sleep quality, and anxiety in hospitalized patients with hip fractures

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20231120060119N1
Enrollment
100
Registered
2023-12-07
Start date
2023-12-22
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Hip fracture. Disorders of bone density and structure

Interventions

Intervention 1: Intervention group: Intervention group: the group will receive progressive muscle relaxation from the next day of surgery for three nights, while the last meal has been at least three

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 65 Years

Inclusion criteria

Inclusion criteria: Diagnosis of hip fractures (based on the diagnosis of an orthopedic specialist in the medical record) age 40-65 No multiple trauma or fracture of both upper and lower limbs Being literate in reading and writing No use of sleeping, sedative anti-depressant, or psychotic drugs in the last 2 months No serious dementia or cognitive dysfunction (based on the patient's or his family's self-report) No drug addiction

Exclusion criteria

Exclusion criteria: Dissatisfaction to enter the study Hospitalization less than 5 days Hospitalization less than 48 hours from admission

Design outcomes

Primary

MeasureTime frame
Sleep quality. Timepoint: Before the intervention, one day after the completion of the intervention. Method of measurement: Numerical rating scale for pain.;Sleep quality. Timepoint: The Pittsburgh Sleep Quality Index. Method of measurement: Before the intervention, one day after the completion of the intervention.;Anxiety. Timepoint: Before the intervention, one day after the completion of the intervention. Method of measurement: The State-Trait Anxiety Inventory.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParvaneh Vasli

Shahid Beheshti University of Medical Sciences

parvanehvasli@gmail.com+98 21 8865 5367

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 6, 2026