Safety and Effect on Quality of Life/Work Productivity of Humira in Patients With Rheumatoid Arthritis
- Conditions
- Rheumatoid Arthritis
- Registration Number
- NCT01076205
- Lead Sponsor
- AbbVie (prior sponsor, Abbott)
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 7229
- Moderate to severe active rheumatoid arthritis in adults with insufficient response to disease-modifying antirheumatic drugs
- Inclusive methotrexate
- Moderate to severe active rheumatoid arthritis in adults who have not been treated with methotrexate before; In case of incompatibility with methotrexate, Humira can be used as monotherapy.
- Hypersensitivity against the drug or one of the other ingredients
- Active tuberculosis or other severe infections (e.g. sepsis and opportunistic infections)
- Moderate to severe cardiac insufficiency
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change From Baseline in Number of Missed Working Days Due to Sick Leave in the Past 6 Months 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.
Percentage of Participants With > 5 Missed Working Days Due to Sick Leave in the Past 6 Months 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.
Change From Baseline in Work Productivity and Activity Impairment: Absenteeism 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.Change From Baseline in Work Productivity and Activity Impairment: Presenteeism 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.Change From Baseline in Work Productivity and Activity Impairment: Total Work Productivity Impairment 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.Change From Baseline in Work Productivity and Activity Impairment: Total Activity Impairment 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.Change From Baseline in Work Activity Index (WAI) 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).
Change From Baseline in Disease Activity Score - 28 Joints (DAS28) 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.
Change From Baseline in Tender Joint Count 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.
Change From Baseline in Swollen Joint Count 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.
EuroQol-5 Dimensions (EQ-5D) Scores 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):
* agility/mobility
* self-care
* usual activities
* pain, bodily discomfort
* anxiety, depression
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).Change From Baseline in Euroqol Visual Analog Scale (VAS) 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."
Change From Baseline in Erythrocyte Sedimentation Rate Baseline and 3, 6, 12, 24, 36, 48, and 60 months Change From Baseline in C-reactive Protein Baseline and 3, 6, 12, 24, 36, 48, and 60 months Change From Baseline in Health-Assessment Questionnaire-Disability Index (HAQ-DI) 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.
- Secondary Outcome Measures
Name Time Method Number of Physician Visits in Past 6 Months Baseline, 6, 12, 24, 36, 48, and 60 months Participants self-reported the number of physician visits they had in the past 6 months.
Number of Inpatient Hospitalizations in Past 6 Months Baseline, 6, 12, 24, 36, 48, and 60 months Participants self-reported the number of hospitalizations they had in the past 6 months.
Duration of Inpatient Hospitalizations in Past 6 Months 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.
Number of Days With Impairment of Non-Occupational Activities in Past 6 Months 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.
Duration of Morning Stiffness Baseline and 3, 6, 12, 24, 36, 48, and 60 months Participant's Assessment of Pain 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).
Participant's Assessment of Fatigue 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).
Percentage of Participants Taking Concomitant RA Medications 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.
Patient Assessment of Adalimumab Therapy 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:
* Considerably better
* Better
* About the same
* Worse
* Noticeably worse