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NCT06063603 · ADVERSE EVENTS

Adverse events

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.

Adverse events occurred during the study; they are not necessarily caused by treatment. Serious events are not interchangeable with severe/grade 3–4 events. These safety populations may differ from efficacy populations.

Collection time frame
Up to 60 days
Other-event reporting threshold
0%

Groups II and III did not participate in the intervention and were not enrolled to the study. Adverse events were not collected from the provider and interventionalist participants in Group II or III.

Participants affected / participants at risk, as reported
Safety groupSerious eventsOther eventsDeaths
Group I (Pain Management)

See detailed description. Acupuncture Therapy: Undergo acupuncture therapy Cancer Pain Management: Receive pain clinic referral Cognitive Behavior Therapy: 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 PCM and 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

0 / 510 / 510 / 51
Group II (Intervention Providers)

Group II participants were not enrolled to the study and participated only in study development.

0 / 00 / 00 / 0
Group III (Medical Oncology Providers)

Group III participants were not enrolled to the study and participated only in study development.

0 / 00 / 00 / 0

Group identifiers: EG000: Group I (Pain Management) · EG001: Group II (Intervention Providers) · EG002: Group III (Medical Oncology Providers)

Serious adverse events

Event terms and counts are source-reported; expand to read more. A reporting threshold may omit less frequent events.

    Other reported adverse events

    Event terms and counts are source-reported; expand to read more. A reporting threshold may omit less frequent events.

      Complete source fields
      description
      Groups II and III did not participate in the intervention and were not enrolled to the study. Adverse events were not collected from the provider and interventionalist participants in Group II or III.
      event Groups
      1. deaths Num Affected
        0
        deaths Num At Risk
        51
        description
        See detailed description. Acupuncture Therapy: Undergo acupuncture therapy Cancer Pain Management: Receive pain clinic referral Cognitive Behavior Therapy: 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 PCM and 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
        EG000
        other Num Affected
        0
        other Num At Risk
        51
        serious Num Affected
        0
        serious Num At Risk
        51
        title
        Group I (Pain Management)
      2. deaths Num Affected
        0
        deaths Num At Risk
        0
        description
        Group II participants were not enrolled to the study and participated only in study development.
        id
        EG001
        other Num Affected
        0
        other Num At Risk
        0
        serious Num Affected
        0
        serious Num At Risk
        0
        title
        Group II (Intervention Providers)
      3. deaths Num Affected
        0
        deaths Num At Risk
        0
        description
        Group III participants were not enrolled to the study and participated only in study development.
        id
        EG002
        other Num Affected
        0
        other Num At Risk
        0
        serious Num Affected
        0
        serious Num At Risk
        0
        title
        Group III (Medical Oncology Providers)
      frequency Threshold
      0
      time Frame
      Up to 60 days

      Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

      Preserved source evidence · Not medical advice