Skip to main content
Clinical Trials/NCT04644757
NCT04644757CompletedNot Applicable

Feasibility and Efficacy of Remotely Monitored Home-based Listening to Preferred Music for Pain in Older Adults With Low Back Pain: A Pilot Study of Feasibility and Acceptability

The University of Texas Health Science Center, Houston1 site in 1 country20 target enrollmentStarted: May 13, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
20
Locations
1
Primary Endpoint
Adherence rate

Study Overview

Brief Summary

The purpose of this study is to examine the feasibility and acceptability of listening to 20 minutes of preferred style of music twice-daily for 4 consecutive days on pain among 20 community-dwelling older adults with lower back pain (LBP)

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
65 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •self-report of Lower back pain (LBP)
  • •LBP in the past 3 months with an average rating of at least 30 on a 0 - 100 NRS for pain
  • •intact cognition
  • •no plans to change their pain medication regimens during the study time
  • •can read and understand English
  • •can travel to the study center
  • •agree to sign an informed consent

Exclusion Criteria

  • •deaf or have severe hearing loss
  • •pregnant or lactating
  • •have an implantable pain-reducing device
  • •history of hospitalization within the preceding year for psychiatric illness
  • •diagnosis of Raynaud's disease
  • •have a functional limitation that requires the use of an ambulatory aid such as a cane, walker, or wheelchair
  • •history of brain surgery, brain tumor, or stroke
  • •severe depression (PROMIS Depression T-score ≥ 70) (Kroenke et al., 2020)
  • •severe anxiety (PROMIS Anxiety ≥ 70) (American Psychiatric Association, 2013)
  • •Mini-Mental State Examination score less than 24 (Creavin, Wisniewski, Noel-Storr, et al., 2016)

Arms & Interventions

Treatment

Experimental

Intervention: Music Listening (Other)

Outcomes

Primary Outcomes

Adherence rate

Time Frame: 6 months from start of study

Assessed as number completing all measures divided by number enrolled

Enrollment rate: Assessed as number enrolled or number who met inclusion criteria

Time Frame: 6 months from start of study

Attrition rate

Time Frame: 6 months from start of study

Assessed as number not completing the study divided by number enrolled at baseline

Treatment acceptability: Measured by the treatment acceptability and preference scale(TAP

Time Frame: Baseline

Assess perceived acceptability of treatment using TAP in four categories of appropriateness, effectiveness, suitability, and willingness to adhere on a scale ranging from 0 (not at all) to 4 (very much).

Treatment acceptability: Measured by the treatment acceptability and preference scale(TAP)

Time Frame: 5 days after baseline(1 day after completion of intervention)

Assess perceived acceptability of treatment using TAP in four categories of appropriateness, effectiveness, suitability, and willingness to adhere on a scale ranging from 0 (not at all) to 4 (very much).

Secondary Outcomes

  • Anxiety as measured by the Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety Short Form(Baseline)
  • Depression as measured by the Patient-Reported Outcomes Measurement Information System (PROMIS) Depression Short Form(Baseline)
  • Pain as measured by the numerical rating scale (NRS)(post intervention (day 5))
  • Change in brain activation in the motor and somatosensory cortex as measured by functional near-infrared spectroscopy (fNIRS)(Baseline and post-intervention (Day 5))
  • Change in conditioned pain modulation (CPM)(Baseline and post-intervention (Day 5))
  • Change in heart rate variability (HRV)(Baseline and post-intervention (Day 5))
  • Pain as measured by the numerical rating scale (NRS)(Baseline)
  • Pain as measured by the numerical rating scale (NRS)(day 1)
  • Pain as measured by the numerical rating scale (NRS)(day 2)
  • Pain as measured by the numerical rating scale (NRS)(day 3)
  • Pain as measured by the numerical rating scale (NRS)(day 4)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Setor K. Sorkpor

Student

The University of Texas Health Science Center, Houston

Study Sites (1)

Loading locations...

Similar Trials