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Psychosocial Support for Pre-operative Pain and Distress

Psychosocial Support for Pre-operative Pain and Distress

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03665727
Acronym
Mind-Body JRA
Enrollment
727
Registered
2018-09-11
Start date
2018-06-04
Completion date
2019-09-23
Last updated
2020-05-27

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

Conditions

Acute Pain

Brief summary

The purpose of this randomized study is to determine the impact of three different types of psychosocial support delivered by mental health professionals to pre-operative joint replacement patients. This study will examine the differential effects of brief mindfulness training, hypnostic suggestion, and cognitive behavioral pain psychoeducation for pre-operative patients, with a supplemental nonrandomized usual care comparison group.

Interventions

BEHAVIORALMindfulness

The 15 minute mindfulness session is a scripted mindfulness exercise that incorporates mindfulness principles of intentionally paying attention to present-moment experience in a non-judgmental fashion.

BEHAVIORALSuggestion

The 15 minute suggestion session is a scripted suggestion exercise that incorporates imagery and suggestions for changes in cognition, emotion, and body sensations.

BEHAVIORALPsychoeducation

The 15 minute psychoeducation session is a supportive session in which behavioral coping strategies for pain management are discussed.

Sponsors

University of Utah
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Clinical assessors were masked at postoperative follow-up

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* English-speaking males or females * 18 years old or older * patients within the University of Utah Hospital system * patients attending the Joint Replacement Academy to prepare for either hip or knee replacement surgery

Exclusion criteria

* Altered mental status due to delirium, psychosis, or pharmacological sedation as determined by clinical assessment.

Design outcomes

Primary

MeasureTime frameDescription
Pain Unpleasantness Numeric Rating ScaleImmediately prior to and following interventionSingle Likert scale item ranging from 0-10, with 0 indicating no pain and 10 representing the most unpleasant pain imaginable.
Pain Intensity Numeric Rating ScaleImmediately prior to and following interventionSingle Likert scale item ranging from 0-10, with 0 indicating no pain and 10 representing the most intense pain imaginable.

Secondary

MeasureTime frameDescription
Anxiety Numeric Rating ScaleImmediately prior to and following interventionSingle Likert scale item ranging from 0-10, with 0 indicating no anxiety and 10 representing very anxious.
Nondual Awareness Dimensional Assessment - StateImmediately prior to and following interventionThree Likert scale item ranging from 0-30, with 0 indicating no nondual awareness and 10 representing complete nondual awareness. Items can also be used individually. Item one is a single Likert scale item ranging from 0-10, with 0 indicating no relational unity and 10 representing complete relational unity. Item two is a single Likert scale item ranging from 0-10, with 0 indicating no annihilational unity and 10 representing complete annihilational unity. Item three is a single Likert scale item ranging from 0-10, with 0 indicating no bliss and 10 representing complete bliss.
Sensation Manikin Body Sensation ReportImmediately prior to and following interventionThe ratio of pleasant to unpleasant bodily sensations reported on a sensation manikin. Ratio scores below 1 indicate unpleasant sensations predominate in the body and ratio scores above 1 indicate pleasant scores predominate.
Postoperative Patient Reported Outcomes Measurement Information System (PROMIS) Physical Functioning Item Bank, v2.0During the 6 weeks prioir to surgery and at the 6-week outpatient follow-up appointment.The PROMIS physical functioning computer assisted test draws from a bank of 123 items all scored on a 5 point Likert scale. T-Score distributions are standardized such that a 50 represents the average (mean) for the US general population, and the standard deviation around that mean is 10 points. A high score better physical functioning.
Pain Medication Desire Numeric Rating ScaleImmediately prior to and following interventionSingle Likert scale item ranging from 0-10, with 0 indicating no desire for pain medication and 10 representing a strong desire for pain medication.

Other

MeasureTime frameDescription
Present Moment Awareness Numeric Rating Scale (Manipulation Check)Immediately prior to and following interventionSingle Likert scale item ranging from 0-10, with 0 indicating no awareness of the present and 10 representing complete awareness of the present moment.
Decentering Numeric Rating Scale (Manipulation Check)Immediately prior to and following interventionSingle Likert scale item ranging from 0-10, with 0 indicating no decentering and 10 representing a completely decentered perspective.

Countries

United States

Outcome results

None listed

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