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Comparison of the effect two methods of rhythmic breathing and music therapy on pain intensity, anxiety and hemodynamic indicators of patients after orthopedic surgery

Comparison of the effect two methods of rhythmic breathing and music therapy on pain intensity, anxiety and hemodynamic indicators of patients after orthopedic surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20231024059844N1
Enrollment
90
Registered
2023-11-23
Start date
2023-11-06
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

Orthopedic surgery. Encounter for orthopedic aftercare following scoliosis surgery

Interventions

Intervention 1: Intervention group:For the first group (rhythmic breathing), before the operation (when the patient s condition is necessary), the researcher will teach how to perform rhythmic breathi

Sponsors

Zabol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Consent to participate in the research Having at least reading and writing literacy Not suffering from mental disorders based on medical records No history of taking psychiatric drugs and anti-anxiety drugs in the last 6 months Age 30 to 70 years Performing orthopedic surgery on the lower limb or placing an internal fixator No previous history of fracture and orthopedic surgery A fracture in a lower limb or the need for a fixator in a limb No trauma to the head, chest and abdomen No hearing disorders Hospitalization after surgery No respiratory disease (asthma, bronchitis, etc.) No diabetes No drug addiction Analgesic injection more than 4 hours before measuring the desired variables

Exclusion criteria

Exclusion criteria: Withdrawal from participating in the research Need for re-surgery during the study Getting other diseases while doing research The use of local drugs or other measures (hypnosis, distraction, etc.) that can affect pain, anxiety, or hemodynamic indicators during the study. Analgesic injection less than 4 hours before measuring the desired variables

Design outcomes

Primary

MeasureTime frame
Intensity of pain. Timepoint: The first 12 hours and the second 12 hours after surgery. Method of measurement: Pain Visual Scale Questionnaire.;The level of anxiety. Timepoint: The first 12 hours and the second 12 hours after surgery. Method of measurement: Spielberger questionnaire.;Pulse count. Timepoint: The first 12 hours and the second 12 hours after surgery. Method of measurement: Pulse count in one minute.;Blood pressure. Timepoint: The first 12 hours and the second 12 hours after surgery. Method of measurement: Measurement by pressure gauge.

Secondary

MeasureTime frame
Intensity of pain. Timepoint: The first 12 hours and the second 12 hours after surgery. Method of measurement: Visual analog scale questionnaire.;The level of anxiety. Timepoint: The first 12 hours and the second 12 hours after surgery. Method of measurement: Spielberger questionnaire.;Pulse count. Timepoint: The first 12 hours and the second 12 hours after surgery. Method of measurement: Pulse count in one minute.;Blood pressure. Timepoint: The first 12 hours and the second 12 hours after surgery. Method of measurement: Measurement by pressure gauge.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMitra Zarei

Zabol University of Medical Sciences

mytrazary754@gmail.com+98 71 3620 3184

Outcome results

None listed

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