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NCT05698914
Telehealth Mindfulness After Spine Surgery
NA trial testing Telehealth mindfulness-based intervention (MBI) in Lumbar Spine Surgery in 67 participants. Completed in 11 July 2025.
11 July 2025
Quick facts
| Lead sponsor | Vanderbilt University Medical Center |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 67 |
| Start date | 22 February 2023 |
| Primary completion | 11 July 2025 |
| Estimated completion | 11 July 2025 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Telehealth mindfulness-based intervention (MBI)
- Telehealth Education
Conditions studied
- Lumbar Spine Surgery — all drugs for Lumbar Spine Surgery →
- Chronic Low-back Pain — all drugs for Chronic Low-back Pain →
- Postsurgical Pain — all drugs for Postsurgical Pain →
Sponsor
Vanderbilt University Medical Center
Who can join
18 and older, any sex, with Lumbar Spine Surgery or Chronic Low-back Pain. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this pilot clinical trial is to compare two behavioral interventions for patients who are recovering from lumbar spinal surgery for a degenerative spine condition. The study aims to answer the following questions: 1. Is it feasible and acceptable to deliver the interventions and conduct the study procedures in this patient population? 2. Do the interventions benefit patients with regard to pain-related, functional, opioid use, and psychosocial outcomes at 3 and 6 months after surgery, and does one intervention have more benefit than the other? Participants will be asked to do the following: 1. Complete self-report questionnaires online before spine surgery, and around 2 weeks, 3 months, and 6 months after spine surgery. 2. Complete a sensory pain task before spine surgery, and around 2 weeks, 3 months, and 6 months after spine surgery. 3. Around two weeks after surgery, participants will be randomly assigned by chance to one of two behavioral interventions - Mindfulness or Education. Participants will then be asked to attend 8, weekly sessions with a study treatment coach over telehealth (online with camera and microphone).
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT05698914
- Europe PMC full search
- ASCO Meeting Library
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Related trials
Other recruiting trials for Lumbar Spine Surgery
Currently open trials in the same condition.
- NCT07406997 — Rehabilitation With Empowered STrategies to Optimize REcovery · NA · recruiting
- NCT07061067 — Affection of Symptoms Duration on Outcomes of Lumbar Spine Surgery · recruiting
- NCT05680259 — Assessment of the Effects of Maela Connected Follow-up on Well-being and Pain After Lumbar Spine Surgery · NA · active not recruiting
Other Vanderbilt University Medical Center trials
Trials by the same sponsor.
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- NCT07527273 — Cognitive Enhancement in Recurrent Depression (The COG-D-R Study) · NA · not yet recruiting
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- NCT07431541 — Topical Carboxytherapy Paste Following Microneedling · Phase 1, PHASE2 · not yet recruiting
- NCT07224711 — The Impact of Perioperative Lidocaine Infusions on Enhanced Recovery After Non-Cardiac Surgery · Phase 4 · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05698914 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Vanderbilt University Medical Center
- Last refreshed: 5 February 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05698914.
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