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CompletedNCT01663909Updated Aug 13, 2012

Pain Management Using Guided Imagery for Adolescents Post-spinal Fusion

An interventional study of Guided imagery intervention in Pain and Scoliosis, sponsored by St. Justine's Hospital. Completed at 1 site in Canada. Open to participants aged 11 Years to 20 Years. Per ClinicalTrials.gov, last updated 2012-08-13.

Sponsored by St. Justine's Hospital · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
11 Years to 20 Years
Sex
All
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Study 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.

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Conditions studied

  • Pain
  • Scoliosis

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Keywords

  • Pain
  • Scoliosis
  • Rehabilitation
  • Cognitive-behavioral interventions
  • Adolescents
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In context

Scoliosis

594 studies on the registry are indexed under Scoliosis; 139 are open to participants now.

This study's enrollment of 40 is close to the median of 44 across 344 interventional studies indexed under Scoliosis.

Browse Scoliosis studies →

Lead sponsor

St. Justine's Hospital is the lead sponsor of 155 studies on the registry; 27 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
11 Years to 20 Years
Sexes eligible
All
Accepts 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

Exclusion Criteria:

  • Diagnosed with a moderate cognitive deficit or severe mental retardation
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
40 participants (actual)

Study arms

  • No intervention
    Standard care
  • Experimental
    Guided imagery

    Behavioral: Guided imagery intervention

Interventions

  • BehavioralGuided imagery intervention

    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.

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What researchers measure

Primary outcomes

  1. Level of pain intensity

    Pain 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.

    Time frame: Level of pain intensity at two weeks after the surgery

Secondary outcomes

  1. Level of anxiety

    Anxiety 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.

    Time frame: Level of anxiety from 24-hrs before the surgery, to two weeks and to one month after the surgery

  2. Level of coping

    Coping strategies of adolescents regarding their pain management were also measured pre-operatively (24 hrs before surgery), at two weeks and one month post-surgery.

    Time frame: Level of coping from Baseline (pre-operative), to two weeks and to one month after the surgery

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Study locations

1 site
  • CHU Ste-Justine Hospital
    Montreal, Quebec H3T 1C5, Canada
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 13, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01663909
Lead sponsor
St. Justine's Hospital
Responsible party
Sylvie Charette (Clinical Nurse Specialist, St. Justine's Hospital) — Principal investigator
First posted
Aug 13, 2012
Start date
May 2010
Primary completion
Sep 2011
Completion
Dec 2011
Last update
Aug 13, 2012

Study contacts

Sylvie Le May, RN, PhD
study director · Université de Montréal

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2012. You cannot join it, but the record below documents what was studied.

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