Anxiety Acute, IUD Insertion Complication, Pain, Acute
Conditions
Keywords
Intrauterine Device, IUD, Anxiety, Pain, Music, Contraception, Visual analog scale, VAS
Brief summary
Although intrauterine devices (IUDs) are a highly effective contraceptive method, fear of pain during insertion is one barrier to use. A review of literature reveals little investigation of interventions for anxiety management during the procedure. Furthermore, evidence of non-pharmacological interventions for both anxiety and pain management is limited. Music has been shown to be effective at reducing anxiety and pain in a variety of contexts, however to the investigators' knowledge, its effectiveness for anxiety and pain relief during the IUD insertion procedure has not been formally examined. This study will therefore examine the effectiveness of listening to music on anxiety and pain during IUD insertion.
Detailed description
The study is a randomized controlled trial of patients at least 16 years of age undergoing an IUD insertion. The experimental group will receive music, self-selected, with a music-playing device prior and during the procedure and the control group will receive standard care. Data for pain and anxiety will be collected prior to the procedure, and during, and after IUD insertion. In addition, a post-procedure questionnaire will be given to patients and providers to ask about satisfaction and acceptability of the intervention.
Interventions
BEHAVIORALMusic listening
Patients will be asked to either use their personal phones to listen to preferred music which is already on their device, or if they do not have a phone or other personal device capable of playing music of their choice, we will use a device (e.g. iPod) to load music of their choice. While in the waiting room, participants will listen to music through headphones/earphones, however they will need to remove their headphones/earphones during the initial consultation with the family physician (explaining risks, etc.), and resume listening to music through the phone speakers once in the examination room as patients will need to be able to hear instructions from the physician during the procedure.
Sponsors
McMaster University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)
Masking description
The investigators and statisticians performing final data analysis will be blinded to the group allocations
Eligibility
Sex/Gender
FEMALE
Age
16 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Sufficient understanding of English to complete questionnaires * Women who will attend the clinic for an IUD insertion and accept to participate in the study
Exclusion criteria
* Women with chronic pain
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in self-reported anxiety (in the moment) | Baseline, immediately after the procedure, immediately after uterine sounding | 100 mm visual analog scale (VAS) measures anxiety reported by patients; values range 0-100 with higher values representing higher anxiety. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in self-reported pain (in the moment) | Baseline, immediately after uterine sounding, immediately after insertion, immediately after the procedure | 100 mm visual analog scale (VAS) measures pain reported by patients; values range 0-100 with higher values representing higher pain. |
| Change in anxiety | Baseline, immediately after the procedure | The trait anxiety subscale of the State-Trait Anxiety Inventory (Spielberger et al.,1983) will be used to measure trait anxiety. It contains 20 items, each item is rated on a 4-point scale (not at all, somewhat, moderately so, very much so), with higher values representing higher anxiety. Scores range from 20-80 (higher scores represent higher trait anxiety). |
| Complications related to IUD insertion procedure | Immediately after the procedure | Patients and providers are asked to identify any significant adverse reactions experienced (by the patient) during the IUD insertion procedure (e.g., bleeding, vasovagal responses) with open-ended survey developed for the study. |
Other
| Measure | Time frame | Description |
|---|---|---|
| Provider satisfaction and acceptability | At study end, approximately 4 months | Open-ended questionnaire developed for the study asking provider about their opinions regarding the use of music during IUD insertion, whether they would recommend the intervention to patients. |
| Patient satisfaction and acceptability | Immediately after the procedure | Open-ended questionnaire developed for the study asking patient about their opinions regarding the use of music during IUD insertion, whether they would recommend the intervention to friends. |
| Perceived facilitators and barriers | At study end, approximately 4 months | Open-ended questionnaire developed for the study asking the provider whether there are any methods to help implement listening to music during the IUD insertion procedure. |
Countries
Canada
Contacts
Primary ContactRobin Lennox, MD
Outcome results
None listed