A randomised controlled trial of an online aftercare proram in pain rehabilitation

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON27656

Enrollment

142

Registered

2015-12-30

Start date

2016-02-01

Completion date

Unknown

Last updated

2024-06-11

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

Conditions

chronic pain

Interventions

The intervention consists of NaDien, CoCo and a contact module in the experimental condition. NaDien: This program is based on Acceptance & Commitment Therapy. The website and mobile application aim

Eligibility

Inclusion criteria

Inclusion criteria: •Patients aged between 18 and 65 years old •Primary complaint is chronic musculoskeletal pain •Having finished a pain rehabilitation treatment at RCR •Being able to use an online program •Disposal of a smartphone, I-pad or PC •Permission to use data for scientific purposes

Exclusion criteria

Exclusion criteria: Dropped out of rehabilitation program

Design outcomes

Primary

Measure	Time frame
Main study outcome is pain interference measured by the Multidimensional Pain Inventory – subscale pain interference (MPI – interference) (Kerns et al., 1985; Lousberg et al., 1999).	—

Secondary

Measure	Time frame
Pain Intensity measured by the Multidimensional Pain Inventory – subscale pain intensity (MPI – intensity) (Kerns et al., 1985; Lousberg et al., 1999). Psychological distress meadured by Hospital Anxiety Depression Scale (HADS) (Zigmond & Snaith, 1983). Psychological flexibility measured by Psychological inflexibility in Pain Scale (PIPS) (Wicksell et al, 2010; Trompetter et al., 2014).	—

Contacts

Public ContactKMG Schreurs

Roessingh, centrum voor revalidatie

k.schreurs@roessingh.nl053-4875486

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)