City of Hope Medical Center
Duarte, California, 91010, United States
NCT Number: NCT05036408
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.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Duarte, California, 91010, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participate in group psychological intervention
Attend educational session
Other names: Education for Intervention, Intervention by Education, Intervention through Education, Intervention, Educational
Undergo osteopathic manual treatments
Other names: Manipulative and Body-Based Intervention, Manipulative and Body-Based Methods, Manipulative and Body-Based Systems
Participate in occupational therapy
Other names: OT
Participate in physical activity
Participate in physical therapy
Other names: Physiatric Procedure, Physical Medicine Procedure, Physical Therapeutics, Physical Therapy Procedure, Physiotherapy, Physiotherapy Procedure, PT
Ancillary studies
Time frame: 24 months from the intervention date
Feasibility of the program will be determined by the proportion of referred eligible cancer survivors enrolled into the program (at least 50% who are eligible enroll) and the proportion of enrolled patients completed at least half of the intervention.
Time frame: Pre-intervention , End of intervention (6 weeks), 3 months post-intervention
Pain Numerical Rating Scale (NSR) score: patients are asked to circle the number between 0 and 10, zero usually represents 'no pain at all' whereas the upper limit 10 represents 'the worst pain ever possible'.
Time frame: Pre-intervention, End of intervention (6 weeks), 3 months post-intervention
The Pain Self-Efficacy Questionnaire (PSEQ) score: the PSEQ is a 10-item questionnaire, developed to assess the confidence people with ongoing pain have in performing activities while in pain. Scores can range from 0 - 60 and is done by simple addition. High PSEQ scores are strongly associated with clinically-significant functional levels and provide a useful gauge for evaluating outcomes in chronic pain patients. Higher scores (and a higher percentile) represent lower confidence to function with pain.
Time frame: Pre-intervention, End of intervention (6 weeks), 3 months post-intervention
Activities of Daily Living (ADL): Medical Outcomes Study [MOS] subscale, Measures limitations in physical function activities, ranging from bathing and dressing to running.
Time frame: Pre-intervention, End of intervention (6weeks), 3 months post-intervention
Instrumental Activities of Daily Living (iADL): Older American Resources and Services [OARS] subscale, Measures ability to complete activities required to maintain independence, ranging from making telephone calls to money management.
Time frame: Pre-intervention, End of intervention (6 weeks), 3 months post-intervention
Six minutes walk test (6MWT): The 6-min walk test is a submaximal exercise test that entails the measurement of distance (meter) walked over a span of 6 minutes.
Time frame: Pre-intervention, End of intervention (6 weeks), 3 months post-intervention
Ten meter walking test (10mWT): The 10 Meter Walk Test is a performance measure used to assess walking speed in meters per second over a short distance.
City of Hope Medical Center
Other
Cancer Pain Rehabilitation Program in Cancer Survivorship Feasibility Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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