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Phase 1: Randomized Evaluation of a System to Deliver Mobile Cognitive Behavioral Therapy

Phase 1: Randomized Evaluation of a System to Deliver Mobile Cognitive Behavioral Therapy to Lower Pain Catastrophizing Scores

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04836169
Acronym
P1RESPECT
Enrollment
30
Registered
2021-04-08
Start date
2021-10-31
Completion date
2022-05-31
Last updated
2021-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Analgesics, Opioid, Pain, Postoperative

Keywords

pain

Brief summary

The clinical study described in this Clinical Investigation Plan (CIP) will be completed in two stages, Phase I and Phase II. The results of Phase I will confirm patient use of InCaveo's EOA system with integrated mobile CBT but without tapering to improve The Pain Catastrophizing Scale (PCS) scores, and secondarily scores on the VNS pain scale, the Tampa Scale of Kinesiophobia (TSK), and patient satisfaction scores in the subacute period (defined as 2 weeks to 3 months post TKR). Statistically significant positive results on the Pain Catastrophizing Scale (PCS) will trigger phase 2. Phase 1 will also inform the detailed conditions and patient management algorithms for Phase II.

Detailed description

The InCaveo End Opioid Addiction (EOA) System is an integrated pain management therapeutic and opioid tapering system providing alternate treatment options via self-service Cognitive Behavior Therapy (CBT) built into a mobile software app, patient medication usage, and tracking of patient PROs. It is designed to be used alongside Usual Standard of Care using Pill Bottles or to simplify, Usual Care with Pill Bottles (UCPB) treatment practices. The InCaveo EOA System is designed to improve a set of patient outcome measures, primarily Pain Catastrophizing Scale (PCS) and secondarily the Visual Numeric Pain (VNS), Kinesiophobia (TSK) and satisfaction scores while facilitating the ability of patients to taper off their pain medication faster than through the use of USPB in the management of post-operative pain. In order to reduce confounding variables, the study will focus on pain management following a single surgical procedure: Total Knee Replacement (TKR) surgery.

Interventions

DEVICEInCaveo's EOA system with integrated mobile CBT

integrated pain management therapeutic and tapering system including a software apt that manages and tracks patient-reported outcomes, including pain levels, medication use, quality of life

Sponsors

InCaveo
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Randomized parallel-group

Eligibility

Sex/Gender
ALL
Age
55 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

1. Patient has a Pain Catastrophizing Score \>16 2. 55 years of age and older. 3. English speaking. 4. Has a smartphone (iPhone). 5. Able to swallow oral medications. 6. No continuous daily opioid as defined as more than 15 days in the 30 days before surgery. 7. Undergoing TKR surgery. 8. Patients who are willing and able to comply with scheduled visits and study procedures.

Exclusion criteria

1. Diagnosed with Opioid Use Disorder (OUD). 2. Actively using illicit drugs. 3. Allergy to opioids 4. Older than 85 years

Design outcomes

Primary

MeasureTime frameDescription
Pain Catastrophizing Scale (PCS)60 daysA measure of the extent of catastrophizing

Contacts

Primary ContactCynthia Harris, BS
cindy@clinregconsult.com8326776747
Backup ContactMichael A Daniel, MBA
madaniel@clinregconsult.com4154070223

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026