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Pain Management Using Guided Imagery for Adolescents Post-spinal Fusion

The Efficacy of Guided Imagery on Pain, Anxiety, and Coping for Adolescents Post-spinal Fusion

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01663909
Enrollment
40
Registered
2012-08-13
Start date
2010-05-31
Completion date
2011-12-31
Last updated
2012-08-13

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

Conditions

Pain, Scoliosis

Keywords

Pain, Scoliosis, Rehabilitation, Cognitive-behavioral interventions, Adolescents

Brief summary

Surgery to correct scoliosis (spinal fusion)generates a severe pain intensity rending pain management a complex task. Several studies have found out that pharmacological interventions alone were not enough to provide optimal pain management for these patients. The investigators developed a DVD on guided imagery, customized for teenagers, to help them cope better with their pain. The investigators believe that this type of intervention combined with their usual analgesic medication will help them to control their pain and foster rehabilitation.

Interventions

A 30-min DVD was developed which included general information on pain management as well as a section on guided imagery using sounds and images.

Sponsors

St. Justine's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
11 Years to 20 Years
Healthy volunteers
No

Inclusion criteria

* Aged between 11 and 20 years old * Have undergone a posterior/anterior arthrodesis surgery for idiopathic scoliosis * Able to write and understand French * Requires a computer or DVD player at home.

Exclusion criteria

* Diagnosed with a moderate cognitive deficit or severe mental retardation

Design outcomes

Primary

MeasureTime frameDescription
Level of pain intensityLevel of pain intensity at two weeks after the surgeryPain was measured before the patients left the hospital on their 7th postoperative day (T-1, time of discharge from hospital). It was measured again at two week post-discharge (T-2) and also at one month post-discharge (T-3) on their visit to the orthopedic clinic. Our primary outcome was at T-2.

Secondary

MeasureTime frameDescription
Level of anxietyLevel of anxiety from 24-hrs before the surgery, to two weeks and to one month after the surgeryAnxiety was measured as baseline data on the pre-operative visit (24 hrs before surgery). It was also measured at two weeks post-discharge and at one month on the day of the visit to the orthopedic clinic.
Level of copingLevel of coping from Baseline (pre-operative), to two weeks and to one month after the surgeryCoping strategies of adolescents regarding their pain management were also measured pre-operatively (24 hrs before surgery), at two weeks and one month post-surgery.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026