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Effects of transcutaneous electrical nerve stimulation (TENS) on pain due fracture

Effects of transcutaneous electrical nerve stimulation (TENS) on reduction pain feeling after hip and proximal of femoral fractures surgury

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230103057034N1
Enrollment
74
Registered
2023-05-02
Start date
2022-04-03
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Osteoporotic hip and femur fractures. Osteoporosis with current pathological fracture

Interventions

Intervention 1: Intervention group: In the intervention group, after receiving the standard post-surgery treatment, physiotherapy with a device with a frequency of 180-250 volts is performed every mor

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients who, according to the clinical and radiographic findings, suffered a fracture in the pelvis or proximal femur.

Exclusion criteria

Exclusion criteria: Patients who die during surgery or after discharge Patients who do not want to cooperate

Design outcomes

Secondary

MeasureTime frame
Partial weight walking. Timepoint: Before discharge. Method of measurement: The amount of distance traveled in two minutes.;Full weight walkinf. Timepoint: After discharg. Method of measurement: The time required to reach the full weight setup of 10 steps.

Primary

MeasureTime frame
After the surgery, the level of pain is checked with the help of the vas score questionnaire during a 5-day intervention period as explained below: once during the first 24 hours after the surgery, before applying physiotherapy and TENS, and then Immediately before each session of physiotherapy and TENS application, by asking the participant, the intensity of pain at night and at rest, the amount of pain experienced the night before and while resting in bed or sitting in a chair during the day is evaluated.In the following, the pain level is assessed once in two weeks after the surgery when the patient visits the orthopedic clinic. Also, the pain level will be measured once with the help of VAS 3 months after the surgery. Timepoint: once during the first 24 hours after the surgery, before applying physiotherapy and TENS, and then Immediately before each session of physiotherapy and TENS application, by asking the participant, the intensity of pain at night and at rest, the amount of pain experienced the night before and while resting in bed or sitting in a chair during the day is evaluated.In the following, the pain level is assessed once in two weeks after the surgery when the patient visits the orthopedic clinic. Also, the pain level will be measured once with the help of VAS 3 months after the surgery. Method of measurement: VAS questionnaire to measure the pain level of patients: Visual analog scale (VAS) is a tool that is widely used to measure pain. The patient is asked to indicate their perceived pain intensity (usually) along a 100 mm horizontal line and this rating is then measured from the left edge (= VAS score). VAS score correlates well with acute pain level.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadreza Rasouli

Arak University of Medical Sciences

mrr1996@yahoo.com+98 86 3222 2003

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026