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Music therapy on pain and stress reduction during transvaginal ultrasound-guided oocyte retrieval: a randomized controlled trial

Music therapy on pain and stress reduction during transvaginal ultrasound-guided oocyte retrieval: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001657
Enrollment
Unknown
Registered
2011-11-04
Start date
2011-10-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

infertile women undergoing oocyte retrieval

Interventions

A:One group of patient will be offered a MP3 machine with headphone, however, no music will be played.
B:In another group, no MP3 machine with headphone and no music will be offered.

Sponsors

Prince of Wales Hospital, The Chinese University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Patient undergoing transvaginal ultrasound-guided oocyte retrieval

Exclusion criteria

Exclusion criteria: 1. Patient is suffering from following disease: (1) Deaf; (2) Endocrine disease including diabetes mellitus, thyroid, hypothalamic, adrenal problems; (3) On steroid therapy; (4) Salivary gland disease; 2. Smoker or drinker; 3. Refuse or incompetence for informed consent.

Design outcomes

Primary

MeasureTime frame
Assessment of pain by a 100mm linear visual analogous scale (VAS) related to transvaginal ultrasound-guided oocyte retrieval (TUGOR). Patient will be asked to give the satisfaction score regarding the pain control of TUGOR.;The additional of analgesic during and after TUGOR will be recorded.;Blood pressure, heart rate, respiratory rate, oxygen saturation level will be measured in every 10 minutes during TUGOR.;Assessment of anxiety and stress Basal anxiety level will be assessed by the Chinese version of the Spielberger’s State Anxiety Inventory (STAI) (Appendix I);12-item General Health Questionnaire (GHQ-12) (Appendix II) and Beck Depression Inventory (BDI) (Appendix III);Salivary for stress hormone including cortisol and amylase level will be measured before and immediately after TUGOR procedures.;

Secondary

MeasureTime frame
Surgeon’s perception towards adequately of pain and sedation control will be rated using same VAS and satisfactory score.;Assessment of patient satisfaction Patient attitude towards the treatment will be assessed by an 8-item client satisfaction questionnaire (CSQ-8) (Appendix IV).;Experience of post-operative side effect will be recorded.;Sedation and co-operation scale intra-operative sedation and co-operation will be assessed by surgeon of TUGOR and will be scored according to 5-point sedation and co-operation scales.;

Countries

China

Contacts

Public ContactDr. Wai Yee Wong
alicewywong@cuhk.edu.hk+852 26322583

Outcome results

None listed

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