Spots Global Cancer Trial Database for Cancer Pain Rehabilitation Program to Reduce Pain Related Distress, and Reliance of Pain Medication Through Multimodal Nonpharmacological Solutions

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Trial Identification

Brief Title: Cancer Pain Rehabilitation Program to Reduce Pain Related Distress, and Reliance of Pain Medication Through Multimodal Nonpharmacological Solutions

Official Title: Cancer Pain Rehabilitation Program in Cancer Survivorship Feasibility Study

Study ID: NCT05036408

Conditions

Hematopoietic and Lymphoid Cell Neoplasm

Malignant Solid Neoplasm

Interventions

Behavioral, Psychological or Informational Intervention

Educational Intervention

Manipulative and Body-Based Intervention Procedure

Occupational Therapy

Physical Activity

Physical Therapy

Questionnaire Administration

Study Description

Brief Summary: This clinical trial studies the effect of an interdisciplinary program with strong patient involvement on managing long-term chronic pain for cancer survivors. The purpose of this study is to determine whether enrolling patients into an interdisciplinary program can improve mobility with physical and occupational therapy and participation in online group psychotherapy that teaches coping skills to enhance quality of life.

Detailed Description: PRIMARY OBJECTIVE: I. To test the feasibility of an interdisciplinary functional restoration program in cancer survivors with chronic pain and restoring physical function. EXPLORATORY OBJECTIVE: I. To explore the preliminary effect of functional restoration program (FRP) in restoring physical function and reducing pain which ultimately decreases opioid consumption. OUTLINE: Patients participate in the cancer pain rehabilitation program for 6 weeks, including educational sessions over 2 hours once weekly, group psychological interventions, group physical therapy, and 1:1 physical and occupational therapy treatment per the patient's treatment plan. Patients may also undergo osteopathic manual treatments per physical and occupational therapy assessments. After completion of study intervention, patients are followed up at 3 months.