NCT05700747 · ADVERSE EVENTS
Adverse events
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
- From enrollment until end of follow-up (up to 4 months)
- Other-event reporting threshold
- 0%
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Health Through Activity (HTA) Intervention | 0 / 5 | 0 / 5 | 0 / 5 |
Serious adverse events
Other reported adverse events
Complete source fields
- event Groups
- deaths Num Affected
- 0
- deaths Num At Risk
- 5
- description
- Participants will undergo study procedures as outlined: * Complete a baseline survey regarding activity level and quality of life. * Attend 6 weekly study visits at the MGH Institute of Health Professions IMPACT Practice Center. * Attend final study visit and complete the Satisfaction survey and an individual, semi-structured interview with site staff to supply feedback about the program. * After six weeks, complete the Satisfaction survey again.
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 5
- serious Num Affected
- 0
- serious Num At Risk
- 5
- title
- Health Through Activity (HTA) Intervention
- frequency Threshold
- 0
- time Frame
- From enrollment until end of follow-up (up to 4 months)
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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