Enhancing Patient Experience of Pain and Sleep Through Non-Pharmacological Strategies

Comfort Clinical Trial

Official title: Enhancing Patient Experience of Pain and Sleep Through Non-Pharmacological Strategies

Status Enrolling by invitation

Clinical Trial Summary

Comfort can be a physical sensation, a psychological state, or both simultaneously . Patient comfort in an inpatient setting is a subjective state that varies from each individual based on different factors and situations. The Richards-Campbell Sleep Questionnaire (R-CSQ) and the Revised American Pain Society Outcome Questionnaire (APS-POQ-R) are tools that have been developed to assess patient satisfaction and comfort in the hospital setting. The R-CSQ is a scale used to measure different aspects of sleep quality. This scale allows the patient to rate their quality and amount of sleep on a scale of 0-100. The R-CSQ allows the patient to rate six different components of their sleep, including sleep depth, sleep latency, awakenings, returning to sleep, sleep quality, and noise. The APS-POQ-R can be utilized to measure perceived levels of pain in patients. The APS-POQ-R scale is a validated scale that is used in the hospital setting with reliable and consistent results. This scale measures five aspects of a patient's perception and experiences with pain and a sixth aspect including nonpharmacological interventions.

We propose that if patients implement interventions that promote sleep and decrease pain, comfort will be improved.

Clinical Trial Description

Aim(s)/Objective(s)

• Improve patient sleep during their hospital stay.

• Determine patient self-reported pain assessment using non-pharmacologic strategies.

• Determine if the "patient toolkit" improves patient experience of pain and sleep.

Hypothesis 1. Primary Hypothesis Patients' experience of pain and sleep will improve with the implementation of interventions from our "patient toolkit".

.2. Secondary Hypothesis Patients will report an increase in sleep and a decrease in pain after use of the interventions provided in the "patient toolkit".

3. Tertiary Hypothesis Patients will report satisfaction with results gained through implementation of our "patient toolkit".

STUDY DESIGN

• 60 to 80 medical surgical patients per campus (MCMC, MDMC, MMMC, MRMC) will be recruited to participate (total: 240 to 320 patients) Only adult medical surgical patients over the age 20 will be recruited.

• Quasi-experimental, pre-/post-test, repeated measures interventional study

• Length of patients hospital stay will determine length of intervention used; average estimate is a four-day length of stay

• Give pre-assessment the morning after first night of admission (Day 2)

• Participants will receive a toolkit upon informed consent completion that will include intervention strategies (eye mask; ear plugs; puzzle book; adult coloring book; colored pencils; aromatherapy patches; herbal tea bags) and data collection booklet for pre-survey, daily survey, and post-survey

• Data will be collected over 6 to 10 weeks to achieve desired number of participants

• Anticipated completion of study will be December 2021 ;

Related Conditions & MeSH terms

• Comfort

• NCT number: NCT04428164
• Study type: Observational
• Source: Methodist Health System
• Status: Enrolling by invitation
• Start date: February 15, 2022
• Completion date: December 30, 2022