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Lower Extremity Splinting to Manage Pain and Sleep Disturbances Associated With HIV/AIDS Related Peripheral Neuropathy

This study has been completed.
Sponsor:
Collaborators:
Harris County Hospital District
DJO Incorporated
Information provided by (Responsible Party):
Robert Sandoval, Texas Woman's University
ClinicalTrials.gov Identifier:
NCT01419314
First received: August 10, 2011
Last updated: December 5, 2012
Last verified: December 2012
Results First Received: September 13, 2012  
Study Type: Interventional
Study Design: Allocation: Randomized;   Endpoint Classification: Safety/Efficacy Study;   Intervention Model: Parallel Assignment;   Masking: Single Blind (Subject);   Primary Purpose: Treatment
Conditions: HIV
AIDS
Peripheral Neuropathy
Pain
Sleep
Interventions: Device: Splinting application to the lower extremities
Device: Splint liner application

  Participant Flow
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Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
The participants were randomized to use a night application of bilateral lower extremity splints (23 participants) or using the soft liners of the splints only (23 participants). One participant was excluded from the liner group as he failed to disclose a recent diabetes diagnosis.

Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
One of the participants in the liner group was excluded from the study at the beginning as he developed type-II diabetes. The total number of participants in the liner group was thus 22 at baseline.

Reporting Groups
  Description
Splinting Application Participants will be asked to wear a pair of LE night splints for the duration of the study (6 weeks) at night/during sleep only.
Splint Liner Application The liner or protective sheath from the Walkabout™ splint will be applied to the LEs, with the structural frame of the splint removed by the researcher in advance.

Participant Flow for 3 periods

Period 1:   Start of Study
    Splinting Application     Splint Liner Application  
STARTED     23 [1]   22 [2]
COMPLETED     23     22  
NOT COMPLETED     0     0  
[1] minor comfort issues were reported within the first 2 weeks of the trial
[2] No comfort issues reported.

Period 2:   Follow-up at Week 3 of the Trial
    Splinting Application     Splint Liner Application  
STARTED     23 [1]   22 [2]
COMPLETED     17     21  
NOT COMPLETED     6     1  
Withdrawal by Subject                 3                 1  
Lost to Follow-up                 3                 0  
[1] 3 participants discontinued the trial, 3 failed to return for additional follow-ups.
[2] one participant failed to return for the 3 week follow-up

Period 3:   Follow-up at Week 6 of the Trial
    Splinting Application     Splint Liner Application  
STARTED     17     21 [1]
COMPLETED     16 [2]   19  
NOT COMPLETED     1     2  
Lost to Follow-up                 1                 2  
[1] 2 participants did not return for their final follow-up
[2] 2 people who missed the first follow-up, returned for the final follow-up at week 6 (n=18).



  Baseline Characteristics
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Population Description
Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
No text entered.

Reporting Groups
  Description
LE Splints Group Participants were asked to wear a pair of LE night splints for the duration of the study (6 weeks) at night/during sleep only.
Splint Liner Application The liner or protective sheath from the Walkabout™ splint was applied to the LEs, with the structural frame of the splint removed by the researcher in advance.
Total Total of all reporting groups

Baseline Measures
    LE Splints Group     Splint Liner Application     Total  
Number of Participants  
[units: participants]
  23     22     45  
Age  
[units: participants]
     
<=18 years     0     0     0  
Between 18 and 65 years     23     22     45  
>=65 years     0     0     0  
Age  
[units: years]
Mean ± Standard Deviation
  50.65  ± 8.04     46.09  ± 7.71     48.42  ± 8.13  
Gender  
[units: participants]
     
Female     9     10     19  
Male     14     12     26  
Race/Ethnicity, Customized  
[units: participants]
     
American Indian or Alaska Native     0     0     0  
Asian     0     1     1  
Native Hawaiian or Other Pacific Islander     0     0     0  
Black or African American     12     12     24  
White     9     6     15  
Latino     2     3     5  
Unknown or Not Reported     0     0     0  
CD4 [1]
[units: cells/mm3]
Mean ± Standard Deviation
  586.13  ± 233.64     446.09  ± 232.54     517.67  ± 241.07  
Log Viral load [2]
[units: Log (copies/ml)]
Log Mean ± Standard Deviation
  2.25  ± 1.08     1.96  ± 0.75     2.10  ± 0.93  
Years living with HIV [3]
[units: years]
Mean ± Standard Deviation
  11.30  ± 6.01     10.32  ± 7.62     10.82  ± 6.79  
Pain scores [4]
[units: Scores on a 0-100 scale.]
Mean ± Standard Deviation
  61.35  ± 20.98     60.16  ± 14.35     60.77  ± 17.85  
Sleep Scores [5]
[units: Scores on a 0-21 scale]
Mean ± Standard Deviation
  14.13  ± 3.89     15.14  ± 4.68     14.62  ± 4.28  
Function- Forward reach [6]
[units: Centimeters (cm)]
Mean ± Standard Deviation
  35.31  ± 6.45     36.88  ± 8.36     36.07  ± 7.37  
Function-Walking Distance [7]
[units: Meters (m)]
Mean ± Standard Deviation
  246.00  ± 133.71     241.89  ± 151.46     243.99  ± 141.04  
[1] The most recent CD4 cell counts were extracted from the medical record.
[2] The most recent measured HIV viral load (log viral load) was extracted from the medical record. Measured in viral copies/ml on a logarithmic scale with 1.48 log/ml representing undetectable viral load levels for the viral load test conducted in our site (less than 50 copies/ml)
[3] The number of years living with HIV was calculated by subtracting the year of diagnosis to the year of sutdy enrollment.
[4] Neuropathic Pain Scale (NPS) score, where a score of "0" equates to "no pain" and "100" is the maximum neuropathic pain score possible. The scale score is computed by totaling all 10 pain sub-scales, each individually scored from 0-10.
[5] Pittsburgh Sleep Quality Index (PSQI),this is a 0-21 score scale with 21/21 denoting maximum sleep disturbances. The PSQI is scored by adding all seven sub-scales, each with a maximum score of three. A score greater than 5/21 characterizes the individual as a "poor sleeper."
[6] The average of 3 reaching trials are reported. One participant in the liner group had extreme reaching values (>3 standard deviation from the mean) and was excluded from the report (n=22). Longer distances in this test represent better volitional control of balance in the sagittal plane. Reaching distances >30 cm are considered to be within normal limits.
[7] The 6 minute walk distance was collected on all participants. Longer walking distances represent decreased impact on function. Non-HIV cohorts typically are able to walk 400-600m in six-minutes.



  Outcome Measures
  Show All Outcome Measures

1.  Primary:   Pain Scores at Week 3   [ Time Frame: Week 3 ]

2.  Primary:   Pain Scores   [ Time Frame: Week 6 ]

3.  Primary:   Sleep Quality/Quantity Scores (PSQI)   [ Time Frame: week 3 ]
  Hide Outcome Measure 3

Measure Type Primary
Measure Title Sleep Quality/Quantity Scores (PSQI)
Measure Description The Pittsburgh Sleep Quality Index (PSQI) is a ten item questionnaire, covering the following seven components of sleep: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medications, and daytime dysfunctions.
Time Frame week 3  
Safety Issue No  

Population Description
Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
The number of participants returning for the first follow-up with complete data.

Reporting Groups
  Description
Splinting Application Participants were asked to wear a pair of LE night splints for the duration of the study (6 weeks) at night/during sleep only.
Splint Liner Application The liner or protective sheath from the Walkabout™ splint was applied to the LEs, with the structural frame of the splint removed by the researcher in advance.

Measured Values
    Splinting Application     Splint Liner Application  
Number of Participants Analyzed  
[units: participants]
  16     21  
Sleep Quality/Quantity Scores (PSQI)  
[units: Scores ranging 0-21, 0=no disturbances]
Mean ± Standard Deviation
  13.13  ± 4.51     14.29  ± 4.58  

No statistical analysis provided for Sleep Quality/Quantity Scores (PSQI)



4.  Primary:   Sleep Quality/Quantity Scores (PSQI)   [ Time Frame: week 6 ]

5.  Secondary:   Function-Reach   [ Time Frame: week 3 ]

6.  Secondary:   Function-Reach   [ Time Frame: week 6 ]

7.  Secondary:   Function-Walking Distance   [ Time Frame: week 3 ]

8.  Secondary:   Function-Walking Distance   [ Time Frame: week 6 ]


  Serious Adverse Events


  Other Adverse Events


  Limitations and Caveats
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Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
The contrast between the splinting group and liner group was statistically underpowered. The data was collected and analyzed by the primary investigator. The clinical diagnosis of peripheral neuropathy was not confirmed with EMG or punch skin biopsy.


  More Information
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Certain Agreements:  
Principal Investigators are NOT employed by the organization sponsoring the study.
There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.


Results Point of Contact:  
Name/Title: Roberto Sandoval PT
Organization: Texas Woman's University
phone: 713-859-9351
e-mail: rsandoval@mail.twu.edu


Publications:

Responsible Party: Robert Sandoval, Texas Woman's University
ClinicalTrials.gov Identifier: NCT01419314     History of Changes
Other Study ID Numbers: 16196
Study First Received: August 10, 2011
Results First Received: September 13, 2012
Last Updated: December 5, 2012
Health Authority: United States: Institutional Review Board