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Efficacy of Audio-guide Hypnosis compared with standard usual care for Anxiolysis in patients undergo EGD, Multi-center Randomized control trial.

Efficacy of Audio-guide Hypnosis compared with standard usual care for Anxiolysis in patients undergo EGD, Multi-center Randomized control trial.

Status
Unknown
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20241124003
Enrollment
100
Registered
2024-11-24
Start date
2024-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Patient undergo diagnostic Esophagogastroduodenoscopy Esophagogastroduodenoscopy EGD Sedation Hypnosis Hypnotherapy Audio-guided Hypnosis

Interventions

1. In waiting room during local anesthetic drug was apply, Audio file was played (part 1 : Description of EGD protocol ) , (Part 2: Induction of hypnosis ) - total waiting time 25-30 mins 2. Endosco
Experimental Other,No Intervention Other
Audio-guided hypnosis,Standard of Care

Sponsors

The Gastroenterological Association of Thailand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Participants aged over 20 years who have received information about the research project. 2. Participants undergoing diagnostic esophagogastroduodenoscopy (EGD). 3. Participants who can fluently communicate in the Thai language. 4. Participants who consent to receive at least local anesthesia, with the option for rescue intravenous sedation if necessary.

Exclusion criteria

Exclusion criteria: 1. Participants requiring therapeutic procedures, such as hemostasis, endoscopic band ligation, foreign body removal, nasogastric/nasojejunal (NG/NJ) tube insertion, or dilatation. 2. Participants with hearing impairments, including those using hearing aids. 3. Participants with active psychiatric disorders. 4. Participants with underlying medical conditions requiring anesthesiological monitoring. 5. Pregnant or breastfeeding participants. 6. Participants who withdraw from the study.

Design outcomes

Primary

MeasureTime frame
Anxiety on same day Thai Spielberg State-Trait Anxiety Inventory Thai-STAI, Visual Analog Scale Anxiety,Pain and Discomfort on same day Thai Spielberg State-Trait Anxiety Inventory Thai STAI, Visual Analog Scale Pain and Discomfort

Secondary

MeasureTime frame
change in vital signs Regiester point, at wating room, after endoscopy Blood pressure, Heart rate,Sedative drug same day Drug and dose of rescue sedation,Patient and Doctor satisfaction same day Satisfaction score,Complication after endoscopy in same day questionaire and medical record,Rate of Rescue sedation same day Number of patient using sedative drugs

Countries

Thailand

Contacts

Public ContactJarupoj Tirasriwat

Phramongkutklao hospital

elfiez.tj@gmail.com0821954151

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026