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@ctiveHip Tele-rehabilitation System

@ctiveHip: Tele-rehabilitation System for Hip Fracture Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02968589
Acronym
@ctiveHip
Enrollment
70
Registered
2016-11-18
Start date
2017-01-31
Completion date
2018-07-31
Last updated
2018-04-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip Fractures

Keywords

Tele-rehabilitation, Function, Quality of life, Exercise, Occupational Therapy, Physiotherapy, Caregiver burden

Brief summary

The purpose of this study is to determine if the @ctivehip tele-rehabilitation system improves the functional level and quality of life of hip fracture patients and reduce the caregiver burden.

Detailed description

Background: The best option for rehabilitation after a hip fracture is still unclear. The home rehabilitation is one of the options and the use of tele-rehabilitation programs at home could be the option for some patients in the future. The main objective of this study is to improve the functional level and quality of life of hip fracture patients and reduce the caregiver burden using the @ctivehip tele-rehabilitation system. Methods: This project will include hip fracture patients who met the following inclusion criteria: having a high pre-fracture functional level, not having severe cognitive impairment, absence of terminal disease, absence of post-surgery complications, going to live to their home or a relative home at hospital discharge, and signing an informed consent. The criteria to be part of this experimental group will be: having internet at home and a main caregiver with the ability to use the internet (@ctiveHip system). Patients without the internet at home will be part of the no intervention group, and they will receive the usual care, in addition to a triptych with information on recommendations and exercises to do at home. Caregivers of patients of both groups will receive a training session on patient management. Patients will be assessed at 4-weeks and 12 weeks after beginning to use the @ctiveHip system. The primary outcome will be the Functional level, measured by the Functional Independence Measure. The secondary outcomes: quality of life (Euro-qol), physical function (Timed Up and Go, Short Physical Performance Battery, International Fitness Scale), emotional status ( The Hospital Anxiety and Depression Scale ), health status (American Society of Anesthesiologists Score), cognitive status (Mini-mental Test ), fear of falling (Short Falls efficacy scale), pain (visual analogue scale), and caregiver burden of care (Zarit Burden Interview). Discussion: This study has been designed to provide a tele-rehabilitation system which includes a rehabilitation protocol created by a multidisciplinary team of surgeons, occupational therapist, physiotherapist, and sport scientist, to improve the functional level of patients after hip fracture surgery. The @ctiveHip system could be a new low cost treatment option for some hip fracture patients.

Interventions

BEHAVIORALTraining

Sponsors

Complejo Hospitalario Universitario de Granada
CollaboratorOTHER
Andalusian Initiative for Advanced Therapies - Fundación Pública Andaluza Progreso y Salud
CollaboratorOTHER
Universidad de Granada
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients who had hip fracture surgery Having a high pre-fracture functional level Having Internet at home Hospital discharge to their homes or a relative home. A main caregiver who has the ability to use the internet (@ctivehip system) Have signed an informed consent

Exclusion criteria

Presence of severe cognitive impairment Presence of terminal disease Presence of post-surgery complications

Design outcomes

Primary

MeasureTime frameDescription
Functional LevelParticipants will be followed over 12 weeksThe primary outcome will be assessed with the Functional Independence Measure, which is one of the most widely used instruments to measure Functional Level of hip fracture patients.

Secondary

MeasureTime frameDescription
Quality of life12 weeksThe secondary outcome will be assessed with the EuroQoL Quality of Life Questionnaire which is one of the most widely used instruments to measure quality of life of hip fracture patients.
Mobility12 weeksTimed Up and Go test will be used to measure physical function.
Physical Function12 weeksShort Physical Performance Battery will be used to measure physical function.
Fitness12 weeksInternational Fitness Scale will be used to evaluate perceived patient´s overall fitness, cardio-respiratory fitness, muscular fitness, speed-agility and flexibility.
Emotional status12 weeksThe Hospital Anxiety and Depression Scale will be used to evaluate the emotional status
Health Status12 weeksHealth Status will be assessed using the American Society of Anesthesiologists Score
Cognitive status12 weeksMini-mental Test will be used to measure the cognitive status of hip fracture patients.
Fear of falling12 weeksShort Falls Efficacy Scale will be used to assess fear of falling
Pain12 weeksThe pain will be assessed using the Visual Analogue Scale
Caregiver burden12 weeksZarit Burden Interview will be used to evaluate the caregiver burden of care

Countries

Spain

Contacts

Primary ContactPatrocinio Ariza-Vega, PhD
pariza@ugr.es0034637205620

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026