N/A
Completed N=39
Increasing Physical Activity in Older Adults With Osteoarthritis Pain: Examining a Brief Behavioral Intervention
Osteoarthritis, Knee · Osteoarthritis, Hip
Source: ClinicalTrials.gov NCT04490395 ↗
Enrolled (actual)
39
Serious AEs
0.0%
Results posted
Jan 2023
Primary outcomePrimary: Number of Participants Enrolled in the Study — 19; 20 Participants
Summary
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.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants Enrolled in the Study |
19; 20 | — |
| PRIMARY Number of Participants Who Completed the Entire Program |
19; 20 | — |
| PRIMARY Percentage of Participants Who Were Mostly or Very Satisfied With the Intervention |
89 | — |
| SECONDARY Arthritis Pain (AIMS 2 Symptom Subscale) |
13.72; 14.90; 11.78; 14.58 | 0.044 sig |
| SECONDARY Arthritis-related Physical Functioning (AIMS 2 Physical Functioning Subscale) |
6.38; 7.44; 6.64; 7.51 | 0.056 |
| SECONDARY Psychological Distress (AIMS 2 Affect Subscale) |
10.36; 10.37; 10.59; 10.33 | 0.377 |
| SECONDARY Daily Step Count in 7 Day Period |
35712.55; 28165.89; 38268.56; 28154.67 | 0.258 |
| SECONDARY Rapid Assessment of Physical Activity |
3.25; 3.16; 3.47; 2.31 | 0.038 sig |
| SECONDARY Psychological Flexibility |
13.95; 16.21; 14.72; 13.05 | 0.07 |
| SECONDARY Valued Living - Health Domain |
4.11; 4.05; 3.76; 4.88 | 0.43 |
| SECONDARY Valued Living - Leisure Domain |
4.26; 4.60; 4.12; 4.18 | 0.72 |
| SECONDARY Valued Living - Relationship Domain |
3.68; 4.29; 4.00; 4.35 | 0.341 |
| SECONDARY Valued-Living - Work/Community Domain |
3.32; 3.30; 3.65; 3.41 | 0.25 |
Eligibility Criteria
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
Data sourced from ClinicalTrials.gov (NCT04490395). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.