Dietary Salt in Rheumatoid Arthritis
NCT03649178
Arthritis, Arthritis, Rheumatoid
Nashville, Tennessee, United States
View Trial DetailsNCT Number: NCT01076205
The AGIL study was designed to evaluate the effectiveness and safety of adalimumab over 5 years in routine daily clinical practice in Germany, with a focus on the impact of therapy on employment-related outcomes.
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Notify Me18 year–99 year
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Baseline and 6, 12, 24, 36, 48, and 60 months
Primary effectiveness outcomes related to employment were performed in patients who were employed part- or full-time at baseline. Sick leave days were based on patient recall.
Time frame: Baseline, 6, 12, 24, 36, 48, and 60 months
Primary effectiveness outcomes related to employment were performed in patients who were employed part- or full-time at baseline. Sick leave days were based on patient recall.
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
The Work Productivity and Activity Impairment (WPAI) questionnaire for general health is a validated tool in RA consisting of 6 questions, based on patient recall of the previous 7 days. WPAI assesses work time missed due to illness (absenteeism), impairment at work due to health (presenteeism), total work productivity impairment due to health (an aggregate measure of both absenteeism and presenteeism), and total non-occupational activity impairment due to health.
WPAI scores are expressed as impairment percentages, with higher scores indicating worse outcomes.
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
The Work Productivity and Activity Impairment (WPAI) questionnaire for general health is a validated tool in RA consisting of 6 questions, based on patient recall of the previous 7 days. WPAI assesses work time missed due to illness (absenteeism), impairment at work due to health (presenteeism), total work productivity impairment due to health (an aggregate measure of both absenteeism and presenteeism), and total non-occupational activity impairment due to health.
WPAI scores are expressed as impairment percentages, with higher scores indicating worse outcomes.
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
The Work Productivity and Activity Impairment (WPAI) questionnaire for general health is a validated tool in RA consisting of 6 questions, based on patient recall of the previous 7 days. WPAI assesses work time missed due to illness (absenteeism), impairment at work due to health (presenteeism), total work productivity impairment due to health (an aggregate measure of both absenteeism and presenteeism), and total non-occupational activity impairment due to health.
WPAI scores are expressed as impairment percentages, with higher scores indicating worse outcomes.
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
The Work Productivity and Activity Impairment (WPAI) questionnaire for general health is a validated tool in RA consisting of 6 questions, based on patient recall of the previous 7 days. WPAI assesses work time missed due to illness (absenteeism), impairment at work due to health (presenteeism), total work productivity impairment due to health (an aggregate measure of both absenteeism and presenteeism), and total non-occupational activity impairment due to health.
WPAI scores are expressed as impairment percentages, with higher scores indicating worse outcomes.
Time frame: Baseline and 6, 12, 24, 36, 48, and 60 months
The WAI is a tool designed to record the work ability of employees and consists of 7 questions. The modified WAI used in this study included Questions 1, 2, 4, 6, and 7 of the WAI. Question 3, which involves the number of current diseases diagnosed by a physician, was omitted because this parameter was unlikely to reflect change due to treatment. Question 5 (sick leave during the past year) was replaced with the previous question concerning sick leave days.WAI scores range from 7 (worst) to 49 (best).
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, erythrocyte sedimentation rate (ESR), and the patient's assessment of global disease activity are included in the DAS28 score. Scores on the DAS28 range from 0 to 10. A DAS28 score > 5.1 indicates high disease activity, a DAS28 score < 3.2 indicates low disease activity, and a DAS28 score < 2.6 indicates clinical remission.
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Twenty-eight joints were assessed and classified as tender/not tender by pressure and joint manipulation on physical examination.
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Twenty-eight joints were assessed and classified as swollen/not swollen by pressure and joint manipulation on physical examination.
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
The HAQ-DI is a patient-reported assessment of physical function that includes 20 items in eight categories representing a comprehensive set of functional activities, including dressing, eating, walking, and hygiene. Patients are asked about their ability to complete these tasks in the past week using the following categories: without any difficulty (0); with some difficulty (1); with much difficulty (2); and unable to do (3). Scores on each task were summed and averaged to provide an overall score ranging from 0 (best) to 3 (worst), with a higher score representing a high-dependency disability.
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
The EuroQol-5 Dimensions (EQ-5D) is a generic instrument for measuring health-related quality of life. The patient questionnaire consists of two parts. The first part includes statements for the following five areas (dimensions):
For each dimension the patient is asked for a three-level assessment of their health on the current day: "no problems" (1), "some problems" (2), "extreme problems" (3).
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
EuroQol-5 Dimensions (EQ-5D): The EQ-5D is a generic instrument for measuring health-related quality of life. The patient questionnaire consists of two parts. The second part is a vertical, thermometer-like, VAS ranging from 0 to 100 that provides a patient-reported assessment of overall health. Patients are asked to mark how good or bad their health is on that day, with 100 meaning "the best health you can imagine" and 0 meaning "the worst health you can imagine."
Time frame: Baseline, 6, 12, 24, 36, 48, and 60 months
Participants self-reported the number of physician visits they had in the past 6 months.
Time frame: Baseline, 6, 12, 24, 36, 48, and 60 months
Participants self-reported the number of hospitalizations they had in the past 6 months.
Time frame: Baseline, 6, 12, 24, 36, 48, and 60 months
Participants who had been hospitalized were asked how many days they were hospitalized in the past 6 months.
Time frame: Baseline, 6, 12, 24, 36, 48, and 60 months
Patients reported the number of days that sickness affected non-occupational activities in four categories: household, child-rearing/parenting, education, and recreational (free-time). Participants with no impairment were considered to have 0 days.
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Participants were asked to evaluate their level of pain in the past 7 days on a scale from 0 (no pain) to 10 (unbearable pain).
Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Participants were asked to indicate how much they had suffered from abnormal exhaustion and fatigue during the past 7 days on a scale from 0 (none) to 10 (strongly).
Time frame: Baseline to month 60
Assessment of concomitant medications included disease-modifying antirheumatic drugs (DMARDs) (methotrexate, Leflunomid, sulfasalazine), systemic glucocorticoids, non-steroidal anti-inflammatory drugs (NSAIDs), Cox-2 inhibitors (coxibs), analgesics and others.
Time frame: Months 3, 6, 12, 24, 36, 48, and 60
Participants were asked to rate therapy with adalimumab in comparison with other previous therapies according to the following response options:
AbbVie (prior sponsor, Abbott)
Industry
Long Term Documentation of the Safety and Efficacy as Well as the Effects on Quality of Life and Work Productivity in Patients With Rheumatoid Arthritis Under HUMIRA® (Adalimumab) in Routine Clinical Practice (AGIL)
Acronym: AGIL
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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