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Increasing Physical Activity in Older Adults With Osteoarthritis Pain: Examining a Brief Behavioral Intervention

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Duke University

Status

Completed

Conditions

Osteoarthritis, Hip
Osteoarthritis, Knee

Treatments

Behavioral: Engage PA
Other: Treatment as Usual plus (TAU+)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04490395
Pro00105573

Details and patient eligibility

About

The purpose of this study is to evaluate how older adults might benefit from sessions that teach behavioral coping skills for increasing physical activity and reducing interference from arthritis pain. This study will randomize individuals to receive Engage-PA, or continue to receive treatment as usual. Engage-PA involves two sessions (about 45 minutes each) with a study therapist that teaches individuals behavioral skills for increasing daily steps. These behavioral skills include identifying their personal values and instructions on how to pace their daily physical activity to avoid creating severe pain when walking. All participants in the study will wear small devices that track physical activity such as daily steps throughout the study, which also allow participants to see their daily step counts and overall level of activity. All participants will answer a set of questions about how much arthritis gets the way of many important life activities, their success at living in line with their personal values, and how much thoughts, feelings and body sensations get in the way of living a satisfying life. These questions will be asked at the beginning of the study and 6 weeks into the study.

Enrollment

40 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 65 or older
  • English speaking
  • Diagnosis of osteoarthritis in knee or hip
  • Able to ambulate even if assisted with ambulatory device such as walker or cane
  • Endorse worst pain and pain interference as ≥ 3 out of 10 within the last week

Exclusion criteria

  • Planned surgery during study duration that would limit mobility (e.g., due to recommended rehabilitation or recovery period) for more than 3 weeks
  • Current enrollment in cardiac rehabilitation
  • Myocardial infarction in the past 3 months
  • Major surgery requiring limited movement or mobility for recovery within the past 3 months
  • Presence of a serious psychiatric condition (e.g., schizophrenia, suicidal intent) indicated by medical chart, treating medical provider or other staff, or study staff interactions that would contraindicate safe study participation
  • Medical provider indicating that exercise (even walking) should only be medically supervised; as determined by medical record review or patient reported
  • Fall or falls within the last 3 months that led to immediate medical treatment/hospitalization
  • Reported or suspected moderate or severe cognitive impairment subsequently informed by a Folstein Mini-Mental Status Examination of <19

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Engage PA
Experimental group
Treatment:
Behavioral: Engage PA
Treatment as usual plus fitness tracker
Other group
Treatment:
Other: Treatment as Usual plus (TAU+)

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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