Pain Management Support Study for Patients With Advanced Cancer

Advanced Cancer Clinical Trial

Official title:

Mechanisms of Music Therapy to Palliate Pain in Patients With Advanced Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03432247
• Other study ID #: R01NR016681
• Secondary ID: 1R01NR016681-01A
• Status: Completed
• Phase: N/A
• Start date: February 1, 2018
• Est. completion date: December 31, 2021

Study information

• Verified date: February 2022
• Source: Drexel University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Chronic pain is one of the most feared symptoms in people with cancer. Insufficient relief from pharmacological treatments and the fear of side effects are important reasons for the growing use of complementary pain management approaches in cancer care. On such approach is music therapy. Although several studies have demonstrated that music therapy interventions can reduce pain in people with cancer, few studies have examined the therapeutic mechanisms that explain how music therapy interventions lead to improved pain management. The purpose of this study is to examine whether an interactive music therapy intervention improves psychological and social factors that play an important role in chronic pain management in people with advanced cancer. The findings will contribute towards the optimization of music therapy for palliation of chronic pain in people with advanced cancer.

Description:

This study addresses the public health problem of chronic pain as one of the most feared symptoms in people with cancer, with 70% to 90% of patients with advanced disease reporting pain. Unrelieved pain remains a challenge in cancer care. Insufficient relief from pharmacological treatments and the fear of side effects are important reasons for the growing use of complementary pain management approaches in people with cancer. One such approach is music therapy. Although efficacy of music therapy for pain has been established, there are no mechanistic studies clarifying how it works in clinical populations. Thus, there is a lack of knowledge related to 1) therapeutic mechanisms that lead to improvement (mediator effects) and 2) the relationship between patient characteristics and treatment response (moderator effects). Yet, it is well accepted that knowledge of mediators and moderators as well as a validated theory of action (i.e., how the intervention activates the mediators) are needed to optimize psychosocial treatment interventions. Therefore, the overarching goals of this study are to 1) examine mediators and moderators hypothesized to account for the pain-reducing effects of Interactive Music Therapy (IMT) in people with advanced cancer and chronic pain and 2) validate IMT's theory of action. The mediation model to be tested in this study aligns with a biopsychosocial framework to palliation of chronic pain and is based on findings from a preliminary study. The investigators postulate that anxiety, mood, self-efficacy and perceived support mediate the effects of IMT on pain outcomes (i.e. pain intensity and pain interference). In addition, the impact of several moderators on the hypothesized mediation model, namely adult playfulness, perceived musical competence, and treatment expectancy, will be tested. This study uses a mixed methods intervention design in which qualitative data (i.e. semi-structured follow-up interviews) are embedded within a randomized controlled trial. A total of 100 outpatients with advanced cancer and chronic bone pain will be randomized to one of two 6-week treatments: 1) Interactive Music Therapy or 2) Verbal-based support. The mediators and pain outcomes will be measured at baseline and after the fourth and sixth session using self-report measures as well as biomarkers (salivary cortisol, lachrymal dopamine content, serum oxytocin, and plasma β-endorphins). Follow-up interviews with a subsample of 30 participants will enable the investigators to examine the congruence between the hypothesized mediators and moderators and participant explanations of how IMT influences chronic pain management (i.e. theory of action). This study will contribute towards the optimization of music therapy for palliation of chronic pain in people with advanced cancer through a better understanding of the impact of mediators and moderators of IMT on chronic pain management. The results of this study will provide estimated effects sizes of IMT on the mediators and preliminary effect size estimates for the pain outcomes. This information will be instrumental in the development of a subsequent large-scale efficacy trial.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 103
• Est. completion date: December 31, 2021
• Est. primary completion date: December 31, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• male or female outpatients with advanced cancer (Stage 3 & 4; or relapse refractory patients for myeloma)

• diagnosed with locally advanced cancer that has extended to organs/soft tissue or is impinging on or eroding the bone; or bone metastases or soft tissue metastasis

• moderate to severe pain with an average intensity =4 on a 0-10 Numeric Rating Scale (NRS)

• experiencing pain for = 3 months

• Karnofsky Performance score of = 60 or the Eastern Cooperative Group Performance Status (ECOG) equivalent of = 2 (i.e. requires occasional assistance, but is able to care for most of their personal needs)

Exclusion Criteria:

• expected survival = 3 months

• primary central nervous system (CNS) tumor or CNS metastatic disease that impairs concentration, memory, balance or focus that would preclude ability to participate in a 60 minute, recurring activity and completion of self-report measures

• hematologic malignancies except for myeloma which causes significant bone pain

• = 3 weeks post-operation from start of study

• active psychosis or dementia

• inability to speak or write English

• moderate to severe hearing impairment

• current smoking

• current alcohol dependence

Related Conditions & MeSH terms

• Advanced Cancer
• Neoplasms

Intervention

Behavioral:
• Interactive Music Therapy
Six 45-minute individual interactive music therapy (IMT) sessions delivered by a board-certified music therapist. Sessions start with music-guided breathing, imagery, or humming. The music therapist then engages the participant in singing of familiar songs and co-created vocal or instrumental music improvisations based on patient needs. Discussion about the meaning assigned to songs and emotions expressed through the improvisations follow. The IMT experiences are aimed at facilitating emotional expression, offering support through interactive music making, and strengthening inner resources of creativity. In addition, each week the participant learns music-based techniques for self-management of anxiety, stress, mood, and pain.
• Verbal support
Six 45-minute individual sessions delivered by a master's level clinician with training in counseling. The sessions are focused on patient-initiated conversations about their pain, life stressors and the impact on their daily life. The intervener provides nondirective, supportive care by offering supportive, validating statements and reflective listening. The intervener refrains from employing active suggestion, problem-solving or behavioral or cognitive therapy techniques. The verbal support sessions are aimed at providing an empathic, therapeutic environment to facilitate emotional expression and sharing of worries and fears.

Locations

Country	Name	City	State
United States	Cancer Treatment Centers of America (CTCA)	Philadelphia	Pennsylvania
United States	Hahnemann University Hospital	Philadelphia	Pennsylvania
United States	Thomas Jefferson Sidney Kimmel Cancer Center	Philadelphia	Pennsylvania

Sponsors (2)

Lead Sponsor	Collaborator
Drexel University	National Institute of Nursing Research (NINR)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Treatment expectancy	Moderator outcome measured by Credibility/Expectancy Questionnaire (CEQ)	Baseline
Other	Perceived Musical Competence	Moderator outcome measured by two-item questionnaire	Baseline
Other	Adult playfulness	Moderator outcome measured by Short Measure for Adult Playfulness (SMAP)	Baseline
Primary	Pain Intensity	measured by PROMIS® Pain Intensity-Short Form (SF)3a	through study completion, a maximum of 12 weeks
Primary	Pain Interference	measured by PROMIS® Cancer-Pain Interference -SF 6b	through study completion, a maximum of 12 weeks
Primary	Patient Perception of Change	measured by Patient Global Impression of Change Scale (PGIC)	through study completion, a maximum of 12 weeks
Primary	Serum ß-endorphin	biomarker for pain intensity	through study completion, a maximum of 12 weeks
Secondary	Anxiety	Mediator outcome measured by PROMIS® Cancer-Anxiety - SF	through study completion, a maximum of 12 weeks
Secondary	Mood	Mediator outcome measured by Positive and Negative Affect Scale (PANAS)	through study completion, a maximum of 12 weeks
Secondary	Perceived support	Mediator outcome measured by PROMIS® Emotional Support - SF 6a	through study completion, a maximum of 12 weeks
Secondary	Self-efficacy	Mediator outcome measured by PROMIS® Self-Efficacy of Symptoms	through study completion, a maximum of 12 weeks
Secondary	Salivary cortisol	Mediator outcome (biomarker for anxiety)	through study completion, a maximum of 12 weeks
Secondary	Serum oxytocin	Mediator outcome (biomarker for social support)	through study completion, a maximum of 12 weeks
Secondary	Lachrymal dopamine	Mediator outcome (biomarker for mood)	through study completion, a maximum of 12 weeks