Participant flow

Evaluation of a Pain Management Intervention Preparatory to a Future Pragmatic Trial, ASCENT Study · Source last updated 2025-09-18

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

groups

1. description

   See detailed description. Acupuncture Therapy: Undergo acupuncture therapy Cancer Pain Management: Receive pain clinic referral Cognitive Behavior Therapy(CBT): Undergo CBT Educational Intervention: Receive self-guided pain management education materials Exercise: Participate in exercise Interview: Complete interview Massage Therapy: Receive massage Mindfulness Relaxation: Practice mindfulness Pain Therapy: Receive pain treatment/medicine Palliative Therapy: Receive palliative care referral Patient Navigation: Undergo visits with pain care manager (PCM) and community health worker (CHW) for pain management Referral: Receive pain management referrals Spiritual Therapy: Receive spiritual support Spiritual Care Referral: Receive spiritual care referral Survey Administration: Ancillary studies

   id

   FG000

   title

   Group I (Pain Management)

2. description

   Study interventionalists complete an interview on study.

   id

   FG001

   title

   Group 2 (Intervention Providers)

3. description

   Medical oncology providers participate in a focus group on study.

   id

   FG002

   title

   Group 3 (Medical Oncology Providers)

periods

1. milestones

   1. achievements

      1. group Id

         FG000

         num Subjects

         51

      2. group Id

         FG001

         num Subjects

         5

      3. group Id

         FG002

         num Subjects

         3

      type

      STARTED

   2. achievements

      1. group Id

         FG000

         num Subjects

         44

      2. group Id

         FG001

         num Subjects

         0

      3. group Id

         FG002

         num Subjects

         0

      type

      Completed Intake Visit

   3. achievements

      1. group Id

         FG000

         num Subjects

         43

      2. group Id

         FG001

         num Subjects

         0

      3. group Id

         FG002

         num Subjects

         0

      type

      Completed Planning Visit

   4. achievements

      1. group Id

         FG000

         num Subjects

         41

      2. group Id

         FG001

         num Subjects

         0

      3. group Id

         FG002

         num Subjects

         0

      type

      Completed Final Visit

   5. achievements

      1. group Id

         FG000

         num Subjects

         35

      2. group Id

         FG001

         num Subjects

         0

      3. group Id

         FG002

         num Subjects

         0

      type

      Completed Survey

   6. achievements

      1. group Id

         FG000

         num Subjects

         0

      2. group Id

         FG001

         num Subjects

         0

      3. group Id

         FG002

         num Subjects

         3

      type

      Participated in Focus Group

   7. achievements

      1. group Id

         FG000

         num Subjects

         0

      2. group Id

         FG001

         num Subjects

         5

      3. group Id

         FG002

         num Subjects

         0

      type

      Participated in Interventionalist's Interview

   8. achievements

      1. group Id

         FG000

         num Subjects

         35

      2. group Id

         FG001

         num Subjects

         5

      3. group Id

         FG002

         num Subjects

         3

      type

      COMPLETED

   9. achievements

      1. group Id

         FG000

         num Subjects

         16

      2. group Id

         FG001

         num Subjects

         0

      3. group Id

         FG002

         num Subjects

         0

      type

      NOT COMPLETED

   title

   Overall Study

pre Assignment Details

Only Group 1 were actual participants who were enrolled in the study and received the intervention. Data was only collected for Group 1, so this is the only data reported. Group 2 consisted of interventionalists (provided the intervention to Group 1 participants). Group 3 were Medical Oncology providers. Neither Group 2 nor 3 received any intervention or were enrolled in the study. Groups 2 and 3 participated only in study development.

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