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Structural Integration for Chronic Low Back Pain

CompletedNot applicableNCT01322399
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The primary purpose of study is the collection of feasibility data for a larger trial of Structural Integration (SI)(an alternative manual therapy) for chronic low back pain. The secondary purpose is the collection of preliminary data on 1) the therapeutic effect of SI plus usual care versus usual care alone - the hypothesis being the the effect size will be significantly greater in the SI plus usual care arm; and on 2) specific hypothesized mechanisms of that hypothesized therapeutic effect: a) improvements in cognitive behavioral factors; b) improvements in standing balance and gait, and c) improvements in selected blood biomarkers.

Study details

Official title
Structural Integration for Chronic Low Back Pain
Interventions
  • Procedure: Structural Integration
  • Procedure: Usual care
Sponsor
Spaulding Rehabilitation Hospital
Collaborators
National Center for Complementary and Integrative Health (NCCIH)
Start date
2010-12
Primary completion
2013-08
Sex
All
Age range
from 18 Years to 65 Years
Results posted
No results posted in this snapshot
Countries
United States
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Chronic low back pain patient-rated \>=3 on a VAS (0-10) with retrospective duration of at least 6 months * Low back pain attributed to mechanical as opposed to infectious, neoplastic or inflammatory causes * Age 18-65 * English speaking * Male or female * Mental capacity sufficient to provide informed consent * Able to commit to up to 27 study meetings over a period of 5 months. Exclusion Criteria: * Impairment of hearing, speech, vision, mobility or English fluency sufficient to interfere with participation in the study * Current or anticipated receipt of payments from Workmen's Compensation or other insurance for disability attributed to low back pain. * Reports any prior treatment with Structural Integration (Rolf or other varieties, including "structural massage") * Plans to initiate additional treatment for back pain during the period of the study other than usual rehabilitation care provided at Spaulding Medford clinic, particularly massage or other manual therapy (e.g. chiropractic, osteopathic) * Unresolved musculoskeletal pathology of the lower limbs * Pregnancy * Clinical judgment by Spaulding Medford medical director that the candidate will require either surgery or epidural analgesia within the next five months. * Alcohol of substance abuse * Any implanted medical device (e.g. cardio-pacemaker, shunts) * Prior discectomy or implantation of rods, screws or plates (bulging disc without radicular pain is not exclusionary; hip or shoulder replacement is not exclusionary) * Current medication with coumadin or prednisone, chronic use of steroid medications, daily use of narcotic analgesics. * Current diagnosis with any of the following 1. Balance problems due to vestibular or other neurological impairments 2. Osteoporosis (osteopenia is not exclusionary) 3. Fibromyalgia 4. Severe or progressive neurological deficits, including neuromotor impairment 5. Any hypercoagulation condition 6. Eczema, skin infections, deep vein thrombosis 7. Burns or other acute trauma including unhealed bone fractures or open wounds. 8. Psychiatric illness not well controlled, or current episode of exacerbated major depressive disorder. * Any other major medical condition that has not been stabilized, or that would impair the patient's ability to complete the activities required by the study * Body Mass Index \>= 40

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01322399