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Completed

NCT Number: NCT01076205

Safety and Effect on Quality of Life/Work Productivity of Humira in Patients With Rheumatoid Arthritis

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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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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

Treatment and study plan

Primary outcomes

  1. Change From Baseline in Number of Missed Working Days Due to Sick Leave in the Past 6 Months

    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.

  2. Percentage of Participants With > 5 Missed Working Days Due to Sick Leave in the Past 6 Months

    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.

  3. Change From Baseline in Work Productivity and Activity Impairment: Absenteeism

    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.

  4. Change From Baseline in Work Productivity and Activity Impairment: Presenteeism

    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.

  5. Change From Baseline in Work Productivity and Activity Impairment: Total Work Productivity Impairment

    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.

  6. Change From Baseline in Work Productivity and Activity Impairment: Total Activity Impairment

    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.

  7. Change From Baseline in Work Activity Index (WAI)

    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).

  8. Change From Baseline in Disease Activity Score - 28 Joints (DAS28)

    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.

  9. Change From Baseline in Tender Joint Count

    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.

  10. Change From Baseline in Swollen Joint Count

    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.

  11. Change From Baseline in Erythrocyte Sedimentation Rate

    Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months

  12. Change From Baseline in C-reactive Protein

    Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months

  13. Change From Baseline in Health-Assessment Questionnaire-Disability Index (HAQ-DI)

    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.

  14. EuroQol-5 Dimensions (EQ-5D) Scores

    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):

    • 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).

  15. Change From Baseline in Euroqol Visual Analog Scale (VAS)

    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."

Secondary outcomes

  1. Number of Physician Visits in Past 6 Months

    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.

  2. Number of Inpatient Hospitalizations in 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.

  3. Duration of Inpatient Hospitalizations in 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.

  4. Number of Days With Impairment of Non-Occupational Activities in 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.

  5. Duration of Morning Stiffness

    Time frame: Baseline and 3, 6, 12, 24, 36, 48, and 60 months

  6. Participant's Assessment of Pain

    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).

  7. Participant's Assessment of Fatigue

    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).

  8. Percentage of Participants Taking Concomitant RA Medications

    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.

  9. Patient Assessment of Adalimumab Therapy

    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:

    • Considerably better
    • Better
    • About the same
    • Worse
    • Noticeably worse

Sponsors and collaborators

Lead sponsor

AbbVie (prior sponsor, Abbott)

Industry

Registry information

Official study title

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

Important dates

Study start
2009
Primary completion
2017
Study completion
2017
First posted
Feb 26, 2010
Registry last updated
Feb 7, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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