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N/A Completed N=63 Treatment

Adaptability and Resilience in Aging Adults-2

Source: ClinicalTrials.gov NCT04068922 ↗
Enrolled (actual)
63
Serious AEs
0.0%
Results posted
Jul 2024
Primary outcomePrimary: Session-level Engagement — 6.3 score on a scale

Summary

Chronic low back pain is a major health concern among older adults and is associated with increased economic, functional, and psychological burden. Resilience has been highlighted as a crucial factor in positive health-related functioning, and a growing body of literature supports the use of resilience-based interventions in chronic pain. Therefore, the goals of this project are to examine the feasibility and acceptability of a resilience intervention for chronic low back pain among older adults.

Outcome Measures

OutcomeResultp-value
PRIMARY
Session-level Engagement
6.3 —
PRIMARY
Treatment Satisfaction
3.4 —
PRIMARY
Treatment Credibility and Expectancy
7.7 —
PRIMARY
Satisfaction With Intervention Content
2.9 —
PRIMARY
Intervention Commencement Rate
59 —
PRIMARY
Participant Retention
50 —
PRIMARY
Questionnaire Feasibility
96.8 —
PRIMARY
Home Activity Feasibility
4.6 —

Eligibility Criteria

Inclusion Criteria

  • Age 60 and older
  • Low back pain on at least half the days over the previous 6 months
  • Average daily back pain score ≥3 on a 0-10 numerical rating scale
  • At least moderate (≥3/10) CLBP-related interference on a 0-10 numerical rating scale
  • Able to read/write in English

Exclusion Criteria

  • Current participation in another psychological treatment
  • Severe psychiatric illness not adequately controlled by medication (e.g., schizophrenia, bipolar disorder) or other conditions anticipated to impair intervention engagement (e.g., substance abuse/dependence)
  • Presence of chronic, malignant pain (e.g., HIV, cancer) or systemic inflammatory disease (e.g., rheumatoid arthritis, ankylosing spondylitis, systemic lupus erythematosus, etc.)
  • Significant cognitive impairment on the MoCA
  • If currently taking prescription analgesic or psychotropic medication, must be stabilized on these treatments for ≥4 weeks prior to the baseline assessment
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04068922). 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.

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