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Psychosocial Support for Acute Hospital Pain and Distress

Psychosocial Support for Acute Hospital Pain and Distress

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02590029
Enrollment
244
Registered
2015-10-28
Start date
2015-11-30
Completion date
2018-10-31
Last updated
2020-03-06

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 social workers to patients reporting uncontrolled pain during a hospital stay. This study will examine the differential effects of brief mindfulness training, therapeutic suggestion, and psychoeducation for patients reporting uncontrolled pain.

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
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* English-speaking males or females 18 or older within the University of Utah Hospital system reporting intolerable pain or inadequate pain control on the Clinically Aligned Pain Assessment Tool (CAPA; Donaldson & Chapman, 2013).

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Pain intensity (numeric rating scale)Immediately prior to and following intervention0-10 scale
Pain unpleasantness (numeric rating scale)Immediately prior to and following intervention0-10 scale

Secondary

MeasureTime frameDescription
Relaxation (numeric rating scale)Immediately prior to and following intervention0-10 scale
Desire for opioids (numeric rating scale)Immediately prior to and following intervention0-10 scale
Use of opioid analgesics24 hours prior to and following interventionThe total amount of opioid analgesic use will be computed during the 24 hours prior to and following intervention. Opioid dose will be standardized and calculated using conventional morphine daily equivalent equianalgesic conversion tables.
Use of non-opioid analgesics (NSAID)Within 24 hours prior to and following interventionThe total amount of opioid analgesic use will be computed during the 24 hours prior to and following intervention. NSAID dose will be standardized and calculated using conventional NSAID equianalgesic conversion tables.
Positive body sensations (numeric rating scale)Immediately prior to and following intervention0-10 scale
Anxiety (numeric rating scale)Immediately prior to and following intervention0-10 scale

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 9, 2026