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The effect of Sound Therapy on Pain severity after cesarean section

Clinical trial the effect of sound therapy on severity of pain in women after cesarean section, by spinal anesthesia compared with patients with routine care

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015020114049N2
Enrollment
57
Registered
2015-07-07
Start date
2015-04-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Scores Pain after Sound Therapy. Severe abdominal pain

Interventions

Intervention 1: In the Control group the patient will receive Indomethacin suppository upon entering to ward and pain scores and Hemodynamic signs would be recorded without any further action. Interve
Treatment - Other
In the Control group the patient will receive Indomethacin suppository upon entering to ward and pain scores and Hemodynamic signs would be recorded without any further action.
Intervention group1: in headphone group (without playing any sounds) besides receiving Indomethacin suppository no sound would be played and then pain score and Hemodynamic signs would be measured and
Intervention group 2: The third group which is intervention group using headphone and playing sounds would receive mild nature sounds such as birds, rivers, waterfalls sounds for each individual patie

Sponsors

Vice chancellor for research, Jahrom University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: All the patients who are going to do cesarean section at Motahari hospital affiliated to Jahrom University of Medical Sciences can receive spinal anesthesia. Informed consent for participation in this study is the main criteria for inclusion. Exclusion criteria: Not interested in nature sounds, education under primary school, chronic pains and cancer, Hearing or speech impairment, lack of mental and psychological health, chronic use of painkillers and narcotics, Unstable hemodynamic status, expressing disagreement for continuing the research.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain in the Abdomen and Pelvis. Timepoint: Every 6 hours after surgery Within 48 hours(2 days). Method of measurement: On base of VAS.

Secondary

MeasureTime frame
Vital Signs. Timepoint: Every 6 hours after surgery Within 48 hours(2 days). Method of measurement: Monitoring Blood pressure, Heart Rate, Temperature, Breathing.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarzaneh Mehran

Jahrom University of Medical Sciences

MehranFarzaneh711@gmail.com+98 71 3743 8517

Outcome results

None listed

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