Proof-of-concept Lymfif

NACompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

May 1, 2021

Primary Completion Date

November 1, 2021

Study Completion Date

February 1, 2022

Conditions
Quality of Life
Interventions
BEHAVIORAL

Lymfit intervention

Wearable activity trackers (Fitbit) were given to participants as a motivational tool and for data collection purposes. Participants received a personalized exercise prescription designed by a kinesiologist. Physiologic metrics were collected by the Fitbit monitors and were stored in the Lymfit database. Self-reported questionnaires measuring health outcomes were collected at baseline and post-intervention.

Trial Locations (1)

H3A 2A7

Jewish General Hospital, Montreal

All Listed Sponsors
lead

McGill University

OTHER