Skip to content

The Effects of Guided Imagery on Pain Management, Pre-operative Anxiety, and Recovery in Burn Wound Patients scheduled for Corrective or Reconstructive Surgery: a Randomized Controlled Pilot Study.

The Effects of Guided Imagery on Pain Management, Pre-operative Anxiety, and Recovery in Burn Wound Patients scheduled for Corrective or Reconstructive Surgery: a Randomized Controlled Pilot Study. - The Guided Imagery intervention Study for Burn Injuries: The GISBI study.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON34532
Enrollment
50
Registered
2010-12-24
Start date
2011-03-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

burn injury burn wound patients in need of Corrective or Reconstructive Surgery

Interventions

Intervention group: In addition to standard care: Patients are provided a CD of the guided imagery ("Gezonde Verbeelding", Elsevier publisher) to take home and practice once a day during a period o

Sponsors

Rode Kruis Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: •Written informed consent •Age >= 18 year •Patients with previous burn injury with a need for reconstructive or corrective surgery •Ability to understand and speak the Dutch language •Accessible by phone •Access to CD-player at home

Exclusion criteria

Exclusion criteria: •Known contra-indication to medication used in the standard pain- and general anaesthesia protocol (Midazolam, Paracetamol, Diclofenac, Tramadol, Diprivan, Sufentanil, Morphine, Esmeron and Sevofluran) •Actual psychosis

Design outcomes

Primary

MeasureTime frame
•Amount of used morphine via the PCA-system during the first 3 days after surgery: Amount of morphine via the Patient Controlled Analgesia (PCA) system will be documented in the anesthesia report, medication lists from the recovery room and nursery department.

Secondary

MeasureTime frame
•Use of all post-operative pain medication: Type and amount of used pain medication and medication for anxiety symptoms will be documented daily during the two weeks of the study in the patient diary. •Pre-operative anxiety state: will be measured 7 days before intervention (T0) and at the day of the surgery (T1) using the 6-item APAIS •Self-rated pain: will be noted daily in the patient diary using a 10-cm visual analogue scale (VAS) for pain (ranging from "no pain" to "pain as bad as could possibly be"), from 7 days before to 7 days after surgery. The first 24 hours after surgery VAS scores will be noted every 6 hours according to standard care. •Self-rated recovery: will be noted daily in the patient diary using a 10-cm visual analogue scale (VAS) for self-assessed surgical recovery (ranging from "poor" to "excellent"), during 7 days after surgery. •Feasibility (compliance to intervention). Patients will be asked to record their daily experiences with guided imagery and standard care in the patient diary. A compliance questionnaire is part of the patient diary. Patients will be called by the pain nurse in the intervention period prior to the surgery to monitor compliance. . Involved nurses and medical doctors will be asked to complete an evaluation form about their opinion of practical use of *guided imagery*

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)